Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 3344 |
| ensemblid | ENSG00000170802.17 |
| hgncid | 5281 |
| symbol | FOXN2 |
| name | forkhead box N2 |
| refseq_nuc | NM_002158.4 |
| refseq_prot | NP_002149.2 |
| ensembl_nuc | ENST00000340553.8 |
| ensembl_prot | ENSP00000343633.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 48314682 |
| end | 48379295 |
| strand | + |
| ver | v1.2 |
| region | chr2:48314682-48379295 |
| region5000 | chr2:48309682-48384295 |
| regionname0 | FOXN2_chr2_48314682_48379295 |
| regionname5000 | FOXN2_chr2_48309682_48384295 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 431 | 341 | 80 | 60 | 141 | 14 | 44 | 109 | FOXN2_chr2_48309682_48384295 | FOXN2 | MGPVI others(426): Show |
chr2 | 48309682 | 48384295 |
| a0002 | 0/0 | 431 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | MGPVI others(426): Show |
chr2 | 48309682 | 48384295 |
| a0003 | 0/0 | 431 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | MGPVI others(426): Show |
chr2 | 48309682 | 48384295 |
| a0004 | 0/0 | 431 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | MGPVI others(426): Show |
chr2 | 48309682 | 48384295 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1293 | 215 | 57 | 39 | 74 | 8 | 35 | FOXN2_chr2_48309682_48384295 | FOXN2 | ATGGG others(1288): Show |
chr2 | 48309682 | 48384295 | ||
| a0001c0002 | 0/0 | 1293 | 106 | 11 | 17 | 67 | 5 | 6 | FOXN2_chr2_48309682_48384295 | FOXN2 | ATGGG others(1288): Show |
chr2 | 48309682 | 48384295 | ||
| a0001c0003 | 0/0 | 1293 | 12 | 11 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | ATGGG others(1288): Show |
chr2 | 48309682 | 48384295 | ||
| a0001c0004 | 0/0 | 1293 | 8 | 1 | 3 | 0 | 1 | 3 | FOXN2_chr2_48309682_48384295 | FOXN2 | ATGGG others(1288): Show |
chr2 | 48309682 | 48384295 | ||
| a0002c0005 | 0/0 | 1293 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | ATGGG others(1288): Show |
chr2 | 48309682 | 48384295 | ||
| a0003c0007 | 0/0 | 1293 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | ATGGG others(1288): Show |
chr2 | 48309682 | 48384295 | ||
| a0004c0006 | 0/0 | 1293 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | ATGGG others(1288): Show |
chr2 | 48309682 | 48384295 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 5437 | 159 | 33 | 34 | 55 | 8 | 27 | FOXN2_chr2_48309682_48384295 | FOXN2 | ACTGC others(5432): Show |
chr2 | 48309682 | 48384295 |
| a0001c0001t0002 | 0/0 | 5437 | 12 | 7 | 1 | 0 | 0 | 4 | FOXN2_chr2_48309682_48384295 | FOXN2 | ACTGC others(5432): Show |
chr2 | 48309682 | 48384295 |
| a0001c0001t0004 | 0/0 | 5437 | 17 | 0 | 0 | 17 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | ACTGC others(5432): Show |
chr2 | 48309682 | 48384295 |
| a0001c0001t0005 | 0/0 | 5437 | 14 | 11 | 1 | 0 | 0 | 2 | FOXN2_chr2_48309682_48384295 | FOXN2 | ACTGC others(5432): Show |
chr2 | 48309682 | 48384295 |
| a0001c0001t0008 | 0/0 | 5437 | 2 | 2 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | ACTGC others(5432): Show |
chr2 | 48309682 | 48384295 |
| a0001c0001t0011 | 0/0 | 5437 | 2 | 0 | 0 | 1 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | ACTGC others(5432): Show |
chr2 | 48309682 | 48384295 |
| a0001c0001t0012 | 0/0 | 5437 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | ACTGC others(5432): Show |
chr2 | 48309682 | 48384295 |
| a0001c0001t0014 | 0/0 | 5437 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | ACTGC others(5432): Show |
chr2 | 48309682 | 48384295 |
| a0001c0001t0015 | 0/0 | 5437 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | ACTGC others(5432): Show |
chr2 | 48309682 | 48384295 |
| a0001c0001t0017 | 0/0 | 5437 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | ACTGC others(5432): Show |
chr2 | 48309682 | 48384295 |
| a0001c0001t0018 | 0/0 | 5437 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | ACTGC others(5432): Show |
chr2 | 48309682 | 48384295 |
| a0001c0001t0019 | 0/0 | 5437 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | ACTGC others(5432): Show |
chr2 | 48309682 | 48384295 |
| a0001c0001t0020 | 0/0 | 5437 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | ACTGC others(5432): Show |
chr2 | 48309682 | 48384295 |
| a0001c0001t0021 | 0/0 | 5437 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | ACTGC others(5432): Show |
chr2 | 48309682 | 48384295 |
| a0001c0001t0024 | 0/0 | 5437 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | ACTGC others(5432): Show |
chr2 | 48309682 | 48384295 |
| a0001c0002t0002 | 0/0 | 5437 | 82 | 1 | 11 | 63 | 2 | 5 | FOXN2_chr2_48309682_48384295 | FOXN2 | ACTGC others(5432): Show |
chr2 | 48309682 | 48384295 |
| a0001c0002t0003 | 0/0 | 5436 | 10 | 9 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | ACTGC others(5431): Show |
chr2 | 48309682 | 48384295 |
| a0001c0002t0006 | 0/0 | 5437 | 7 | 0 | 3 | 0 | 3 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | ACTGC others(5432): Show |
chr2 | 48309682 | 48384295 |
| a0001c0002t0009 | 0/0 | 5437 | 2 | 0 | 0 | 2 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | ACTGC others(5432): Show |
chr2 | 48309682 | 48384295 |
| a0001c0002t0010 | 0/0 | 5436 | 2 | 1 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | ACTGC others(5431): Show |
chr2 | 48309682 | 48384295 |
| a0001c0002t0022 | 0/0 | 5436 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | ACTGC others(5431): Show |
chr2 | 48309682 | 48384295 |
| a0001c0002t0023 | 0/0 | 5437 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | ACTGC others(5432): Show |
chr2 | 48309682 | 48384295 |
| a0001c0002t0025 | 0/0 | 5437 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | ACTGC others(5432): Show |
chr2 | 48309682 | 48384295 |
| a0001c0003t0001 | 0/0 | 5437 | 9 | 8 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | ACTGC others(5432): Show |
chr2 | 48309682 | 48384295 |
| a0001c0003t0007 | 0/0 | 5437 | 2 | 2 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | ACTGC others(5432): Show |
chr2 | 48309682 | 48384295 |
| a0001c0003t0016 | 0/0 | 5437 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | ACTGC others(5432): Show |
chr2 | 48309682 | 48384295 |
| a0001c0004t0002 | 0/0 | 5437 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | ACTGC others(5432): Show |
chr2 | 48309682 | 48384295 |
| a0001c0004t0003 | 0/0 | 5436 | 7 | 1 | 3 | 0 | 1 | 2 | FOXN2_chr2_48309682_48384295 | FOXN2 | ACTGC others(5431): Show |
chr2 | 48309682 | 48384295 |
| a0002c0005t0001 | 0/0 | 5437 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | ACTGC others(5432): Show |
chr2 | 48309682 | 48384295 |
| a0003c0007t0013 | 0/0 | 5437 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | ACTGC others(5432): Show |
chr2 | 48309682 | 48384295 |
| a0004c0006t0001 | 0/0 | 5437 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | ACTGC others(5432): Show |
chr2 | 48309682 | 48384295 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0077 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0193 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0004g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0004g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0004g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0005g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0005g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0005g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0005g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0005g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0005g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0008g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0008g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0011g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0011g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0012g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0014g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0015g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0017g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0018g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0019g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0020g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0021g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0001t0024g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0002g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0003g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0006g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0006g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0006g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0006g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0006g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0006g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0006g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0009g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0009g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0010g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0010g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0022g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0023g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0002t0025g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0003t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0003t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0003t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0003t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0003t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0003t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0003t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0003t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0003t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0003t0007g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0003t0007g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0003t0016g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0004t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0004t0003g0001 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0004t0003g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0004t0003g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0004t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0001c0004t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0002c0005t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0003c0007t0013g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| a0004c0006t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0233 | EUR | GBR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0103 | EUR | GBR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG00280 | hp1 | a0001 | c0002 | t0006 | g0243 | EUR | FIN | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG00280 | hp2 | a0001 | c0002 | t0002 | g0261 | EUR | FIN | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG00408 | hp1 | a0001 | c0002 | t0002 | g0322 | EAS | CHS | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0082 | EAS | CHS | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | CHS | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0303 | EAS | CHS | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG00609 | hp1 | a0001 | c0002 | t0002 | g0277 | EAS | CHS | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG00621 | hp2 | a0001 | c0002 | t0002 | g0313 | EAS | CHS | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG00738 | hp2 | a0001 | c0002 | t0003 | g0246 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01069 | hp1 | a0001 | c0001 | t0021 | g0033 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01070 | hp2 | a0001 | c0002 | t0022 | g0238 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01074 | hp1 | a0001 | c0003 | t0001 | g0140 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01074 | hp2 | a0001 | c0002 | t0002 | g0008 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01081 | hp2 | a0001 | c0002 | t0006 | g0242 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01106 | hp2 | a0001 | c0002 | t0002 | g0333 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01109 | hp1 | a0001 | c0002 | t0002 | g0266 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01109 | hp2 | a0001 | c0002 | t0010 | g0247 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01167 | hp2 | a0001 | c0002 | t0002 | g0281 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01169 | hp2 | a0001 | c0002 | t0002 | g0310 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01192 | hp2 | a0001 | c0004 | t0003 | g0001 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0045 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01243 | hp2 | a0001 | c0001 | t0024 | g0202 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01255 | hp2 | a0001 | c0002 | t0006 | g0241 | AMR | CLM | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01257 | hp1 | a0001 | c0002 | t0006 | g0239 | AMR | CLM | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01346 | hp2 | a0001 | c0004 | t0003 | g0043 | AMR | CLM | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | CLM | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0334 | AMR | CLM | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01433 | hp2 | a0001 | c0001 | t0005 | g0003 | AMR | CLM | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01515 | hp1 | a0001 | c0004 | t0003 | g0001 | EUR | IBS | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0212 | EUR | IBS | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0217 | EUR | IBS | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01516 | hp2 | a0001 | c0002 | t0006 | g0240 | EUR | IBS | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0211 | EUR | IBS | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01517 | hp2 | a0001 | c0002 | t0006 | g0244 | EUR | IBS | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01884 | hp1 | a0001 | c0001 | t0012 | g0044 | AFR | ACB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01884 | hp2 | a0001 | c0003 | t0001 | g0142 | AFR | ACB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0029 | AFR | ACB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | ACB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01928 | hp2 | a0001 | c0002 | t0002 | g0259 | AMR | PEL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01952 | hp2 | a0001 | c0002 | t0002 | g0318 | AMR | PEL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01975 | hp1 | a0001 | c0002 | t0002 | g0279 | AMR | PEL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01975 | hp2 | a0001 | c0001 | t0020 | g0116 | AMR | PEL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01978 | hp1 | a0001 | c0002 | t0002 | g0321 | AMR | PEL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02040 | hp1 | a0001 | c0002 | t0002 | g0282 | EAS | KHV | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02040 | hp2 | a0001 | c0001 | t0011 | g0073 | EAS | KHV | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02055 | hp1 | a0001 | c0003 | t0007 | g0011 | AFR | ACB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0330 | EAS | KHV | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02071 | hp1 | a0001 | c0002 | t0002 | g0307 | EAS | KHV | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0319 | EAS | KHV | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02132 | hp1 | a0001 | c0001 | t0004 | g0061 | EAS | KHV | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0269 | EAS | KHV | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | KHV | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02135 | hp2 | a0001 | c0002 | t0009 | g0326 | EAS | KHV | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | ACB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02148 | hp2 | a0001 | c0002 | t0002 | g0312 | AMR | PEL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0270 | EAS | CDX | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02155 | hp2 | a0001 | c0001 | t0004 | g0065 | EAS | CDX | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02258 | hp1 | a0001 | c0004 | t0003 | g0020 | AFR | ACB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0003 | AFR | ACB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | ACB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02451 | hp2 | a0001 | c0003 | t0001 | g0208 | AFR | ACB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02630 | hp1 | a0001 | c0003 | t0001 | g0137 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02717 | hp2 | a0001 | c0002 | t0003 | g0015 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02723 | hp1 | a0002 | c0005 | t0001 | g0094 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02735 | hp2 | a0001 | c0002 | t0006 | g0237 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02809 | hp1 | a0001 | c0001 | t0008 | g0111 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02818 | hp1 | a0001 | c0001 | t0005 | g0046 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02895 | hp1 | a0001 | c0003 | t0001 | g0134 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0002 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0002 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02897 | hp2 | a0001 | c0003 | t0001 | g0133 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0025 | AFR | ESN | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02970 | hp1 | a0001 | c0003 | t0001 | g0148 | AFR | ESN | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ESN | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ESN | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02976 | hp2 | a0001 | c0002 | t0003 | g0248 | AFR | ESN | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03017 | hp2 | a0001 | c0001 | t0005 | g0123 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0023 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03098 | hp1 | a0001 | c0002 | t0003 | g0091 | AFR | MSL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03098 | hp2 | a0001 | c0003 | t0007 | g0010 | AFR | MSL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0024 | AFR | ESN | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03130 | hp2 | a0001 | c0003 | t0016 | g0135 | AFR | ESN | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03139 | hp1 | a0001 | c0001 | t0008 | g0100 | AFR | ESN | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | ESN | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ESN | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03195 | hp2 | a0001 | c0002 | t0003 | g0249 | AFR | ESN | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | MSL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03209 | hp2 | a0001 | c0002 | t0003 | g0256 | AFR | MSL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03225 | hp2 | a0001 | c0002 | t0003 | g0250 | AFR | MSL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0032 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03453 | hp1 | a0001 | c0002 | t0003 | g0251 | AFR | MSL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03453 | hp2 | a0001 | c0001 | t0017 | g0332 | AFR | MSL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | MSL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03490 | hp2 | a0001 | c0004 | t0003 | g0018 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03492 | hp2 | a0001 | c0004 | t0003 | g0001 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | ESN | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0026 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03540 | hp2 | a0001 | c0003 | t0001 | g0181 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03579 | hp1 | a0001 | c0002 | t0003 | g0257 | AFR | MSL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03579 | hp2 | a0003 | c0007 | t0013 | g0145 | AFR | MSL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | STU | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0039 | SAS | STU | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03704 | hp2 | a0001 | c0001 | t0005 | g0163 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0041 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0305 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03831 | hp1 | a0001 | c0001 | t0011 | g0087 | SAS | BEB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | BEB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03834 | hp1 | a0001 | c0002 | t0002 | g0275 | SAS | BEB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03834 | hp2 | a0001 | c0002 | t0002 | g0294 | SAS | BEB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | BEB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0038 | SAS | BEB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03942 | hp1 | a0001 | c0002 | t0002 | g0295 | SAS | BEB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG03942 | hp2 | a0001 | c0001 | t0019 | g0168 | SAS | BEB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG04115 | hp1 | a0001 | c0004 | t0002 | g0021 | SAS | STU | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | STU | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0288 | SAS | STU | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | STU | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | STU | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | STU | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | YRI | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | CHB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18612 | hp2 | a0001 | c0002 | t0002 | g0268 | EAS | CHB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0262 | EAS | CHB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18747 | hp2 | a0001 | c0001 | t0018 | g0105 | EAS | CHB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18906 | hp1 | a0001 | c0002 | t0002 | g0260 | AFR | YRI | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18906 | hp2 | a0001 | c0002 | t0003 | g0252 | AFR | YRI | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18941 | hp2 | a0001 | c0002 | t0002 | g0272 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18942 | hp1 | a0001 | c0002 | t0002 | g0276 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18944 | hp2 | a0001 | c0002 | t0002 | g0048 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18945 | hp1 | a0001 | c0001 | t0004 | g0083 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18945 | hp2 | a0001 | c0002 | t0002 | g0324 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18946 | hp2 | a0001 | c0002 | t0002 | g0278 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18949 | hp2 | a0001 | c0002 | t0002 | g0309 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18950 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18954 | hp1 | a0001 | c0002 | t0002 | g0265 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0055 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18956 | hp2 | a0001 | c0002 | t0002 | g0302 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0317 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18963 | hp1 | a0001 | c0002 | t0002 | g0031 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18969 | hp1 | a0001 | c0001 | t0004 | g0090 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18969 | hp2 | a0001 | c0002 | t0002 | g0293 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18970 | hp1 | a0001 | c0002 | t0002 | g0036 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18972 | hp2 | a0001 | c0002 | t0002 | g0258 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18975 | hp2 | a0001 | c0002 | t0002 | g0327 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18978 | hp1 | a0001 | c0002 | t0002 | g0328 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18980 | hp1 | a0001 | c0002 | t0023 | g0331 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0040 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18982 | hp1 | a0001 | c0002 | t0009 | g0280 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18982 | hp2 | a0001 | c0001 | t0004 | g0088 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18988 | hp2 | a0001 | c0002 | t0002 | g0274 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18989 | hp1 | a0001 | c0002 | t0002 | g0304 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18990 | hp1 | a0001 | c0002 | t0002 | g0301 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18991 | hp1 | a0001 | c0002 | t0002 | g0311 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18992 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18992 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18994 | hp2 | a0001 | c0002 | t0002 | g0325 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18995 | hp1 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18998 | hp1 | a0001 | c0002 | t0002 | g0290 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18998 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19000 | hp2 | a0001 | c0002 | t0002 | g0320 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19002 | hp2 | a0001 | c0002 | t0002 | g0289 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19004 | hp1 | a0001 | c0002 | t0002 | g0299 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19004 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19005 | hp2 | a0001 | c0002 | t0002 | g0316 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19007 | hp2 | a0001 | c0002 | t0002 | g0230 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19011 | hp1 | a0001 | c0001 | t0004 | g0066 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19011 | hp2 | a0001 | c0002 | t0002 | g0306 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19030 | hp1 | a0001 | c0001 | t0014 | g0160 | AFR | LWK | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19030 | hp2 | a0001 | c0001 | t0015 | g0183 | AFR | LWK | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19056 | hp1 | a0001 | c0002 | t0002 | g0285 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19057 | hp1 | a0004 | c0006 | t0001 | g0063 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19057 | hp2 | a0001 | c0002 | t0002 | g0264 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19058 | hp2 | a0001 | c0002 | t0002 | g0263 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19060 | hp1 | a0001 | c0002 | t0002 | g0300 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19060 | hp2 | a0001 | c0002 | t0002 | g0037 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19063 | hp1 | a0001 | c0002 | t0002 | g0287 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19064 | hp1 | a0001 | c0001 | t0004 | g0080 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19064 | hp2 | a0001 | c0002 | t0002 | g0286 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19068 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19072 | hp1 | a0001 | c0002 | t0002 | g0291 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19072 | hp2 | a0001 | c0001 | t0004 | g0081 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19074 | hp1 | a0001 | c0002 | t0002 | g0315 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19075 | hp2 | a0001 | c0002 | t0002 | g0296 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19077 | hp2 | a0001 | c0002 | t0002 | g0297 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19078 | hp1 | a0001 | c0002 | t0002 | g0292 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19079 | hp2 | a0001 | c0002 | t0002 | g0314 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19083 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19083 | hp2 | a0001 | c0002 | t0002 | g0267 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19084 | hp1 | a0001 | c0002 | t0025 | g0059 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19087 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19087 | hp2 | a0001 | c0002 | t0002 | g0284 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19088 | hp1 | a0001 | c0002 | t0002 | g0308 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19089 | hp1 | a0001 | c0002 | t0002 | g0283 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19090 | hp1 | a0001 | c0002 | t0002 | g0298 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19090 | hp2 | a0001 | c0001 | t0004 | g0086 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0027 | AFR | YRI | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | YRI | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA20752 | hp1 | a0001 | c0002 | t0002 | g0271 | EUR | TSI | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0178 | EUR | TSI | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0049 | EUR | TSI | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0102 | EUR | TSI | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | GIH | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | GIH | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01123 | hp1 | a0001 | c0004 | t0003 | g0019 | AMR | CLM | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02109 | hp1 | a0001 | c0003 | t0001 | g0136 | AFR | ACB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0028 | AFR | ACB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG02559 | hp2 | a0001 | c0002 | t0010 | g0245 | AFR | ACB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | USA | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | USA | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18955 | hp1 | a0001 | c0002 | t0002 | g0273 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | LWK | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | LWK | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0193 | REF | REF | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0077 | REF | REF | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:48346477 | T | C | 1 | a0002 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.263T>C | p.Ile88Thr | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/7 | 552/5437 | 263/1296 | 88/431 | chr2 | 48346477 | |||
| chr2:48359093 | C | G | 1 | a0003 | 1 | HG03579.hp2 | missense_variant | MODERATE | c.584C>G | p.Pro195Arg | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/7 | 873/5437 | 584/1296 | 195/431 | chr2 | 48359093 | |||
| chr2:48375195 | G | C | 1 | a0004 | 1 | NA19057.hp1 | missense_variant | MODERATE | c.1048G>C | p.Glu350Gln | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 7/7 | 1337/5437 | 1048/1296 | 350/431 | chr2 | 48375195 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:48375047 | A | G | 1 | a0001c0004 | 8 | HG01123.hp1 HG01192.hp2 HG01346.hp2 others(5): Show |
synonymous_variant | LOW | c.900A>G | p.Glu300Glu | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 7/7 | 1189/5437 | 900/1296 | 300/431 | chr2 | 48375047 | |||
| chr2:48375092 | A | T | 1 | a0001c0003 | 12 | HG01074.hp1 HG01884.hp2 HG02055.hp1 others(9): Show |
synonymous_variant | LOW | c.945A>T | p.Ala315Ala | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 7/7 | 1234/5437 | 945/1296 | 315/431 | chr2 | 48375092 | |||
| chr2:48375113 | C | T | 2 | a0001c0002 a0001c0004 |
114 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(111): Show |
synonymous_variant | LOW | c.966C>T | p.Ser322Ser | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 7/7 | 1255/5437 | 966/1296 | 322/431 | chr2 | 48375113 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:48314754 | G | A | 1 | a0001c0003t0007 | 2 | HG02055.hp1 HG03098.hp2 |
5_prime_UTR_variant | MODIFIER | c.-217G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/7 | 31461 | chr2 | 48314754 | ||||||
| chr2:48328588 | C | G | 2 | a0001c0001t0004 a0001c0002t0025 |
18 | HG00438.hp1 HG02132.hp1 HG02155.hp2 others(15): Show |
5_prime_UTR_variant | MODIFIER | c.-129C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/7 | 17627 | chr2 | 48328588 | ||||||
| chr2:48328681 | A | C | 1 | a0001c0001t0011 | 2 | HG02040.hp2 HG03831.hp1 |
5_prime_UTR_variant | MODIFIER | c.-36A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/7 | 17534 | chr2 | 48328681 | ||||||
| chr2:48375456 | T | C | 1 | a0001c0001t0012 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 7/7 | 13 | chr2 | 48375456 | ||||||
| chr2:48375712 | C | T | 1 | a0001c0002t0010 | 2 | HG01109.hp2 HG02559.hp2 |
3_prime_UTR_variant | MODIFIER | c.*269C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 7/7 | 269 | chr2 | 48375712 | ||||||
| chr2:48375859 | A | G | 1 | a0001c0001t0024 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*416A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 7/7 | 416 | chr2 | 48375859 | ||||||
| chr2:48375886 | G | A | 1 | a0003c0007t0013 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*443G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 7/7 | 443 | chr2 | 48375886 | ||||||
| chr2:48376344 | A | C | 14 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0012 others(11): Show |
142 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(139): Show |
3_prime_UTR_variant | MODIFIER | c.*901A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 7/7 | 901 | chr2 | 48376344 | ||||||
| chr2:48376598 | A | G | 1 | a0001c0001t0020 | 1 | HG01975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1155A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 7/7 | 1155 | chr2 | 48376598 | ||||||
| chr2:48376905 | C | T | 1 | a0001c0001t0019 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1462C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 7/7 | 1462 | chr2 | 48376905 | ||||||
| chr2:48377090 | T | A | 1 | a0001c0001t0021 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1647T>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 7/7 | 1647 | chr2 | 48377090 | ||||||
| chr2:48377418 | A | T | 1 | a0001c0001t0018 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1975A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 7/7 | 1975 | chr2 | 48377418 | ||||||
| chr2:48377578 | G | C | 2 | a0001c0002t0006 a0001c0002t0022 |
8 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2135G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 7/7 | 2135 | chr2 | 48377578 | ||||||
| chr2:48377629 | C | T | 1 | a0001c0002t0023 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2186C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 7/7 | 2186 | chr2 | 48377629 | ||||||
| chr2:48377775 | T | C | 1 | a0001c0001t0014 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2332T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 7/7 | 2332 | chr2 | 48377775 | ||||||
| chr2:48377788 | A | G | 1 | a0001c0001t0017 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2345A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 7/7 | 2345 | chr2 | 48377788 | ||||||
| chr2:48377839 | C | T | 14 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0012 others(11): Show |
130 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*2396C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 7/7 | 2396 | chr2 | 48377839 | ||||||
| chr2:48378024 | T | G | 1 | a0001c0001t0015 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2581T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 7/7 | 2581 | chr2 | 48378024 | ||||||
| chr2:48378143 | C | T | 1 | a0001c0002t0009 | 2 | HG02135.hp2 NA18982.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2700C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 7/7 | 2700 | chr2 | 48378143 | ||||||
| chr2:48378426 | G | T | 1 | a0001c0003t0016 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2983G>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 7/7 | 2983 | chr2 | 48378426 | ||||||
| chr2:48378688 | AT | A | 4 | a0001c0002t0003 a0001c0002t0010 a0001c0002t0022 others(1): Show |
20 | HG00738.hp2 HG01070.hp2 HG01109.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*3260delT | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 7/7 | 3260 | INFO_REALIGN_3_PRIME | chr2 | 48378688 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:48314840 | T | A | 2 | a0001c0003t0007g0010 a0001c0003t0007g0011 |
2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-157+26T>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48314840 | |||||||
| chr2:48314906 | C | T | 2 | a0001c0002t0002g0333 a0001c0002t0002g0334 |
2 | HG01106.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.-157+92C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48314906 | |||||||
| chr2:48314985 | G | C | 1 | a0001c0001t0001g0012 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-157+171G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48314985 | |||||||
| chr2:48315003 | C | A | 1 | a0001c0001t0001g0013 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-157+189C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48315003 | |||||||
| chr2:48315152 | C | A | 1 | a0001c0001t0001g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-157+338C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48315152 | |||||||
| chr2:48315201 | C | T | 1 | a0001c0001t0017g0332 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-157+387C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48315201 | |||||||
| chr2:48315391 | C | T | 1 | a0001c0002t0023g0331 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-157+577C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48315391 | |||||||
| chr2:48315526 | C | G | 78 | a0001c0001t0001g0323 a0001c0001t0001g0329 a0001c0002t0002g0008 others(75): Show |
80 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.-157+712C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48315526 | |||||||
| chr2:48315545 | T | G | 1 | a0001c0002t0003g0015 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-157+731T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48315545 | |||||||
| chr2:48315598 | C | A | 36 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0022 others(33): Show |
40 | HG01069.hp1 HG01123.hp1 HG01192.hp2 others(37): Show |
intron_variant | MODIFIER | c.-157+784C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48315598 | |||||||
| chr2:48315667 | A | T | 3 | a0001c0002t0003g0015 a0001c0002t0003g0256 a0001c0002t0003g0257 |
3 | HG02717.hp2 HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-157+853A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48315667 | |||||||
| chr2:48315747 | C | G | 1 | a0001c0001t0001g0255 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-157+933C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48315747 | |||||||
| chr2:48315793 | C | G | 161 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(158): Show |
167 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.-157+979C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48315793 | |||||||
| chr2:48315810 | G | T | 2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-157+996G>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48315810 | |||||||
| chr2:48316137 | T | C | 1 | a0001c0002t0003g0015 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-157+1323T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48316137 | |||||||
| chr2:48316323 | A | G | 1 | a0001c0001t0001g0210 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-157+1509A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48316323 | |||||||
| chr2:48316509 | A | G | 1 | a0001c0001t0001g0209 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-157+1695A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48316509 | |||||||
| chr2:48316590 | G | A | 1 | a0001c0001t0001g0049 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-157+1776G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48316590 | |||||||
| chr2:48316762 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-157+1948G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48316762 | |||||||
| chr2:48316778 | G | A | 163 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(160): Show |
169 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.-157+1964G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48316778 | |||||||
| chr2:48316893 | C | T | 1 | a0001c0003t0001g0208 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-157+2079C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48316893 | |||||||
| chr2:48316951 | A | ATAG | 292 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0013 others(289): Show |
299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.-157+2137_-157+213 others(7): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48316951 | |||||||
| chr2:48317121 | G | A | 1 | a0001c0002t0003g0091 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-157+2307G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48317121 | |||||||
| chr2:48317240 | G | T | 1 | a0001c0001t0004g0090 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-157+2426G>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48317240 | |||||||
| chr2:48317259 | G | T | 2 | a0001c0002t0002g0047 a0001c0002t0002g0048 |
2 | NA18944.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.-157+2445G>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48317259 | |||||||
| chr2:48317418 | C | T | 4 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(1): Show |
4 | HG00738.hp1 HG01106.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.-157+2604C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48317418 | |||||||
| chr2:48317435 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-157+2621C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48317435 | |||||||
| chr2:48317448 | C | CA | 65 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(62): Show |
69 | HG00099.hp1 HG00438.hp2 HG01069.hp1 others(66): Show |
intron_variant | MODIFIER | c.-157+2646dupA | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48317448 | ||||||
| chr2:48317567 | T | C | 1 | a0001c0002t0002g0259 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-157+2753T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48317567 | |||||||
| chr2:48317584 | C | T | 12 | a0001c0001t0005g0046 a0001c0002t0003g0015 a0001c0002t0003g0246 others(9): Show |
12 | HG00738.hp2 HG01109.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-157+2770C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48317584 | |||||||
| chr2:48317595 | C | CT | 9 | a0001c0001t0001g0089 a0001c0001t0001g0203 a0001c0001t0001g0207 others(6): Show |
10 | HG01928.hp1 HG02056.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.-157+2811dupT | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48317595 | ||||||
| chr2:48317595 | C | CTT | 9 | a0001c0001t0005g0003 a0001c0001t0005g0025 a0001c0001t0005g0026 others(6): Show |
10 | HG00738.hp2 HG01109.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.-157+2810_-157+281 others(6): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48317595 | ||||||
| chr2:48317595 | C | CTTT | 16 | a0001c0001t0001g0051 a0001c0001t0001g0214 a0001c0001t0001g0215 others(13): Show |
16 | HG01070.hp1 HG01516.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.-157+2809_-157+281 others(7): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48317595 | ||||||
| chr2:48317595 | C | CTTTT | 25 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0221 others(22): Show |
25 | HG00438.hp2 HG01069.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.-157+2808_-157+281 others(8): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48317595 | ||||||
| chr2:48317595 | C | CTTTTT | 9 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 others(6): Show |
9 | HG00099.hp1 HG02145.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.-157+2807_-157+281 others(9): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48317595 | ||||||
| chr2:48317595 | C | CTTTTTTT others(1): Show |
7 | a0001c0001t0002g0045 a0001c0001t0012g0044 a0001c0002t0006g0241 others(4): Show |
7 | HG00280.hp1 HG01081.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.-157+2804_-157+281 others(12): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48317595 | ||||||
| chr2:48317595 | CT | C | 139 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0013 others(136): Show |
145 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.-157+2811delT | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48317595 | ||||||
| chr2:48317595 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0002g0016 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-157+2799_-157+281 others(17): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48317595 | ||||||
| chr2:48317595 | CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0001g0213 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-157+2796_-157+281 others(20): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48317595 | ||||||
| chr2:48317595 | CTTTTTTT others(10): Show |
C | 7 | a0001c0001t0001g0014 a0001c0001t0001g0092 a0001c0001t0001g0093 others(4): Show |
7 | HG02723.hp1 HG02970.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.-157+2795_-157+281 others(21): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48317595 | ||||||
| chr2:48317818 | G | C | 2 | a0001c0002t0002g0299 a0001c0002t0002g0300 |
2 | NA19004.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-157+3004G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48317818 | |||||||
| chr2:48317854 | G | A | 8 | a0001c0002t0006g0237 a0001c0002t0006g0239 a0001c0002t0006g0240 others(5): Show |
8 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.-157+3040G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48317854 | |||||||
| chr2:48317858 | C | G | 1 | a0001c0002t0023g0331 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-157+3044C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48317858 | |||||||
| chr2:48317869 | A | G | 1 | a0001c0001t0002g0041 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-157+3055A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48317869 | |||||||
| chr2:48317972 | A | G | 102 | a0001c0001t0001g0159 a0001c0001t0001g0236 a0001c0001t0001g0323 others(99): Show |
104 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.-157+3158A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48317972 | |||||||
| chr2:48318009 | C | T | 1 | a0001c0001t0004g0090 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-157+3195C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48318009 | |||||||
| chr2:48318029 | A | G | 63 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(60): Show |
67 | HG00099.hp1 HG00438.hp2 HG01069.hp1 others(64): Show |
intron_variant | MODIFIER | c.-157+3215A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48318029 | |||||||
| chr2:48318126 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-157+3312C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48318126 | |||||||
| chr2:48318276 | C | G | 1 | a0001c0001t0024g0202 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-157+3462C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48318276 | |||||||
| chr2:48318443 | T | G | 165 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(162): Show |
171 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.-157+3629T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48318443 | |||||||
| chr2:48318448 | A | G | 2 | a0001c0001t0001g0158 a0001c0001t0001g0201 |
2 | HG02896.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-157+3634A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48318448 | |||||||
| chr2:48318495 | C | T | 3 | a0001c0002t0003g0015 a0001c0002t0003g0256 a0001c0002t0003g0257 |
3 | HG02717.hp2 HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-157+3681C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48318495 | |||||||
| chr2:48318646 | A | G | 1 | a0001c0002t0002g0230 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-157+3832A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48318646 | |||||||
| chr2:48318847 | T | A | 3 | a0001c0002t0003g0015 a0001c0002t0003g0256 a0001c0002t0003g0257 |
3 | HG02717.hp2 HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-157+4033T>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48318847 | |||||||
| chr2:48318927 | G | A | 11 | a0001c0002t0003g0015 a0001c0002t0003g0246 a0001c0002t0003g0248 others(8): Show |
11 | HG00738.hp2 HG01109.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-157+4113G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48318927 | |||||||
| chr2:48318930 | T | G | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 |
3 | HG03704.hp1 HG04115.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-157+4116T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48318930 | |||||||
| chr2:48319005 | G | A | 1 | a0001c0002t0002g0301 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-157+4191G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48319005 | |||||||
| chr2:48319042 | A | C | 2 | a0001c0001t0011g0073 a0001c0001t0011g0087 |
2 | HG02040.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.-157+4228A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48319042 | |||||||
| chr2:48319153 | C | CT | 39 | a0001c0001t0001g0014 a0001c0001t0001g0092 a0001c0001t0001g0093 others(36): Show |
39 | HG00642.hp1 HG00738.hp1 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.-157+4351dupT | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48319153 | ||||||
| chr2:48319233 | G | A | 164 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(161): Show |
170 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.-157+4419G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48319233 | |||||||
| chr2:48319260 | G | GA | 63 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(60): Show |
67 | HG00099.hp1 HG00438.hp2 HG01069.hp1 others(64): Show |
intron_variant | MODIFIER | c.-157+4455dupA | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48319260 | ||||||
| chr2:48319372 | T | C | 1 | a0001c0001t0001g0329 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-157+4558T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48319372 | |||||||
| chr2:48319616 | C | CT | 21 | a0001c0001t0001g0200 a0001c0001t0002g0022 a0001c0001t0005g0002 others(18): Show |
23 | HG00280.hp1 HG01069.hp1 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.-157+4817dupT | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48319616 | ||||||
| chr2:48319616 | C | CTT | 144 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(141): Show |
148 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.-157+4816_-157+481 others(6): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48319616 | ||||||
| chr2:48319655 | G | T | 2 | a0001c0003t0007g0010 a0001c0003t0007g0011 |
2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-157+4841G>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48319655 | |||||||
| chr2:48319666 | G | A | 1 | a0001c0001t0014g0160 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-157+4852G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48319666 | |||||||
| chr2:48319673 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-157+4859C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48319673 | |||||||
| chr2:48319757 | C | T | 4 | a0001c0001t0001g0235 a0001c0002t0003g0015 a0001c0002t0003g0256 others(1): Show |
4 | HG02717.hp2 HG03209.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-157+4943C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48319757 | |||||||
| chr2:48319785 | A | AT | 23 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(20): Show |
23 | HG00733.hp1 HG00733.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.-157+4997dupT | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48319785 | ||||||
| chr2:48319785 | AT | A | 18 | a0001c0001t0001g0051 a0001c0001t0001g0098 a0001c0001t0001g0099 others(15): Show |
18 | HG00280.hp2 HG01069.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.-157+4997delT | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48319785 | ||||||
| chr2:48319785 | ATT | A | 16 | a0001c0001t0001g0159 a0001c0002t0002g0260 a0001c0002t0003g0015 others(13): Show |
16 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.-157+4996_-157+499 others(6): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48319785 | ||||||
| chr2:48320163 | A | T | 90 | a0001c0001t0001g0159 a0001c0001t0001g0236 a0001c0001t0001g0323 others(87): Show |
92 | HG00280.hp2 HG00408.hp1 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.-157+5349A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48320163 | |||||||
| chr2:48320190 | A | G | 10 | a0001c0001t0001g0007 a0001c0001t0001g0050 a0001c0001t0001g0144 others(7): Show |
11 | HG02109.hp2 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-157+5376A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48320190 | |||||||
| chr2:48320247 | A | T | 1 | a0001c0004t0003g0020 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-157+5433A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48320247 | |||||||
| chr2:48320304 | A | T | 160 | a0001c0001t0001g0159 a0001c0001t0001g0213 a0001c0001t0001g0214 others(157): Show |
166 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.-157+5490A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48320304 | |||||||
| chr2:48320327 | G | C | 1 | a0001c0001t0001g0210 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-157+5513G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48320327 | |||||||
| chr2:48320369 | C | T | 1 | a0001c0001t0021g0033 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-157+5555C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48320369 | |||||||
| chr2:48320373 | C | G | 2 | a0001c0003t0001g0148 a0001c0003t0001g0208 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-157+5559C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48320373 | |||||||
| chr2:48320438 | A | C | 8 | a0001c0002t0006g0237 a0001c0002t0006g0239 a0001c0002t0006g0240 others(5): Show |
8 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.-157+5624A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48320438 | |||||||
| chr2:48320538 | C | G | 1 | a0001c0001t0001g0072 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-157+5724C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48320538 | |||||||
| chr2:48320608 | A | G | 3 | a0001c0002t0002g0299 a0001c0002t0002g0300 a0001c0002t0002g0324 |
3 | NA18945.hp2 NA19004.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-157+5794A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48320608 | |||||||
| chr2:48320612 | C | T | 162 | a0001c0001t0001g0159 a0001c0001t0001g0213 a0001c0001t0001g0214 others(159): Show |
168 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.-157+5798C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48320612 | |||||||
| chr2:48320683 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-157+5869A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48320683 | |||||||
| chr2:48320716 | T | C | 1 | a0001c0004t0003g0043 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-157+5902T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48320716 | |||||||
| chr2:48320750 | T | C | 1 | a0001c0001t0001g0235 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-157+5936T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48320750 | |||||||
| chr2:48320767 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-157+5953C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48320767 | |||||||
| chr2:48320816 | A | G | 1 | a0001c0002t0002g0295 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-157+6002A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48320816 | |||||||
| chr2:48321009 | T | C | 1 | a0001c0001t0001g0101 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-157+6195T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48321009 | |||||||
| chr2:48321240 | T | G | 8 | a0001c0002t0006g0237 a0001c0002t0006g0239 a0001c0002t0006g0240 others(5): Show |
8 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.-157+6426T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48321240 | |||||||
| chr2:48321303 | G | A | 158 | a0001c0001t0001g0159 a0001c0001t0001g0213 a0001c0001t0001g0214 others(155): Show |
164 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.-157+6489G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48321303 | |||||||
| chr2:48321338 | G | T | 2 | a0001c0002t0006g0240 a0001c0002t0006g0244 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-157+6524G>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48321338 | |||||||
| chr2:48321350 | C | T | 1 | a0001c0003t0001g0142 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-157+6536C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48321350 | |||||||
| chr2:48321594 | TTTTAGTA others(29): Show |
T | 2 | a0001c0002t0003g0250 a0001c0002t0003g0251 |
2 | HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-157+6856_-156-685 others(40): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48321594 | ||||||
| chr2:48321867 | T | A | 1 | a0001c0001t0001g0074 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-156-6694T>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48321867 | |||||||
| chr2:48321927 | A | T | 1 | a0001c0001t0001g0097 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-156-6634A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48321927 | |||||||
| chr2:48322034 | C | T | 1 | a0001c0002t0002g0040 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-156-6527C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48322034 | |||||||
| chr2:48322137 | G | A | 10 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0003 others(7): Show |
12 | HG01433.hp2 HG01891.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.-156-6424G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48322137 | |||||||
| chr2:48322167 | C | G | 1 | a0001c0001t0015g0183 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-156-6394C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48322167 | |||||||
| chr2:48322479 | A | C | 1 | a0001c0002t0002g0294 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-156-6082A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48322479 | |||||||
| chr2:48322658 | A | C | 1 | a0001c0002t0002g0322 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-156-5903A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48322658 | |||||||
| chr2:48323358 | G | A | 99 | a0001c0001t0001g0159 a0001c0001t0001g0214 a0001c0001t0001g0231 others(96): Show |
101 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.-156-5203G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48323358 | |||||||
| chr2:48323439 | G | A | 52 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(49): Show |
54 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.-156-5122G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48323439 | |||||||
| chr2:48323493 | G | T | 11 | a0001c0002t0003g0015 a0001c0002t0003g0246 a0001c0002t0003g0248 others(8): Show |
11 | HG00738.hp2 HG01109.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-156-5068G>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48323493 | |||||||
| chr2:48323549 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-156-5012C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48323549 | |||||||
| chr2:48323592 | T | G | 1 | a0001c0002t0002g0304 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-156-4969T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48323592 | |||||||
| chr2:48323598 | G | T | 5 | a0001c0004t0003g0001 a0001c0004t0003g0018 a0001c0004t0003g0019 others(2): Show |
7 | HG01123.hp1 HG01192.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.-156-4963G>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48323598 | |||||||
| chr2:48323631 | G | C | 161 | a0001c0001t0001g0159 a0001c0001t0001g0213 a0001c0001t0001g0214 others(158): Show |
167 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.-156-4930G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48323631 | |||||||
| chr2:48324194 | A | AT | 63 | a0001c0001t0001g0014 a0001c0001t0001g0092 a0001c0001t0001g0093 others(60): Show |
63 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.-156-4349dupT | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48324194 | ||||||
| chr2:48324194 | A | ATTT | 11 | a0001c0001t0001g0235 a0001c0001t0005g0002 a0001c0001t0005g0003 others(8): Show |
13 | HG01433.hp2 HG01891.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.-156-4351_-156-434 others(7): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48324194 | ||||||
| chr2:48324194 | A | ATTTT | 35 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0213 others(32): Show |
37 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.-156-4352_-156-434 others(8): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48324194 | ||||||
| chr2:48324194 | A | ATTTTT | 16 | a0001c0001t0001g0053 a0001c0001t0001g0218 a0001c0001t0001g0219 others(13): Show |
16 | HG01123.hp2 HG01358.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-156-4353_-156-434 others(9): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48324194 | ||||||
| chr2:48324227 | C | T | 2 | a0001c0002t0002g0299 a0001c0002t0002g0300 |
2 | NA19004.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-156-4334C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48324227 | |||||||
| chr2:48324240 | GC | G | 162 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(159): Show |
168 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.-156-4319delC | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48324240 | ||||||
| chr2:48324355 | T | C | 2 | a0001c0003t0001g0133 a0001c0003t0001g0134 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-156-4206T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48324355 | |||||||
| chr2:48324413 | C | T | 10 | a0001c0001t0002g0017 a0001c0001t0002g0035 a0001c0001t0002g0045 others(7): Show |
12 | HG01123.hp1 HG01192.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.-156-4148C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48324413 | |||||||
| chr2:48324555 | T | G | 1 | a0001c0001t0001g0097 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-156-4006T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48324555 | |||||||
| chr2:48324783 | A | G | 1 | a0001c0001t0001g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-156-3778A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48324783 | |||||||
| chr2:48324835 | G | A | 1 | a0001c0002t0003g0256 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-156-3726G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48324835 | |||||||
| chr2:48324990 | C | T | 28 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(25): Show |
30 | HG01069.hp1 HG01123.hp1 HG01192.hp2 others(27): Show |
intron_variant | MODIFIER | c.-156-3571C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48324990 | |||||||
| chr2:48325095 | T | C | 1 | a0001c0001t0001g0149 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-156-3466T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48325095 | |||||||
| chr2:48325157 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-156-3404G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48325157 | |||||||
| chr2:48325407 | ATG | A | 12 | a0001c0001t0002g0016 a0001c0001t0002g0032 a0001c0001t0002g0038 others(9): Show |
12 | HG01069.hp1 HG02145.hp2 HG03239.hp1 others(9): Show |
intron_variant | MODIFIER | c.-156-3142_-156-314 others(6): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48325407 | ||||||
| chr2:48325522 | T | C | 1 | a0001c0001t0005g0026 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-156-3039T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48325522 | |||||||
| chr2:48325708 | T | C | 1 | a0001c0002t0003g0091 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-156-2853T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48325708 | |||||||
| chr2:48325768 | G | T | 2 | a0001c0003t0007g0010 a0001c0003t0007g0011 |
2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-156-2793G>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48325768 | |||||||
| chr2:48325841 | T | G | 8 | a0001c0001t0001g0012 a0001c0001t0001g0102 a0001c0001t0001g0103 others(5): Show |
8 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.-156-2720T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48325841 | |||||||
| chr2:48325844 | C | CT | 55 | a0001c0001t0001g0096 a0001c0001t0001g0130 a0001c0001t0001g0131 others(52): Show |
57 | HG00280.hp1 HG00738.hp2 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.-156-2695dupT | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48325844 | ||||||
| chr2:48325844 | CT | C | 13 | a0001c0001t0001g0049 a0001c0001t0001g0054 a0001c0001t0001g0056 others(10): Show |
13 | HG01496.hp1 HG02897.hp2 HG03710.hp2 others(10): Show |
intron_variant | MODIFIER | c.-156-2695delT | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48325844 | ||||||
| chr2:48326007 | C | T | 1 | a0001c0002t0002g0289 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-156-2554C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48326007 | |||||||
| chr2:48326069 | C | T | 1 | a0001c0002t0002g0288 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-156-2492C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48326069 | |||||||
| chr2:48326070 | A | G | 135 | a0001c0001t0001g0159 a0001c0001t0001g0213 a0001c0001t0001g0214 others(132): Show |
139 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-156-2491A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48326070 | |||||||
| chr2:48326094 | C | T | 126 | a0001c0001t0001g0159 a0001c0001t0001g0213 a0001c0001t0001g0214 others(123): Show |
130 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.-156-2467C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48326094 | |||||||
| chr2:48326140 | G | A | 1 | a0001c0002t0002g0299 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-156-2421G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48326140 | |||||||
| chr2:48326165 | C | T | 25 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0030 others(22): Show |
27 | HG01069.hp1 HG01123.hp1 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.-156-2396C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48326165 | |||||||
| chr2:48326316 | A | T | 25 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0030 others(22): Show |
27 | HG01069.hp1 HG01123.hp1 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.-156-2245A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48326316 | |||||||
| chr2:48326489 | AAG | A | 26 | a0001c0001t0001g0224 a0001c0001t0002g0016 a0001c0001t0002g0017 others(23): Show |
28 | HG01069.hp1 HG01123.hp1 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.-156-2065_-156-206 others(6): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48326489 | ||||||
| chr2:48326893 | C | A | 1 | a0001c0001t0018g0105 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-156-1668C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48326893 | |||||||
| chr2:48326906 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-156-1655A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48326906 | |||||||
| chr2:48327052 | G | A | 159 | a0001c0001t0001g0159 a0001c0001t0001g0213 a0001c0001t0001g0214 others(156): Show |
165 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.-156-1509G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48327052 | |||||||
| chr2:48327060 | G | T | 1 | a0001c0001t0001g0157 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-156-1501G>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48327060 | |||||||
| chr2:48327111 | T | A | 1 | a0001c0001t0001g0053 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-156-1450T>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48327111 | |||||||
| chr2:48327118 | C | T | 2 | a0001c0002t0003g0250 a0001c0002t0003g0251 |
2 | HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-156-1443C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48327118 | |||||||
| chr2:48327146 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-156-1415G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48327146 | |||||||
| chr2:48327299 | A | T | 8 | a0001c0002t0006g0237 a0001c0002t0006g0239 a0001c0002t0006g0240 others(5): Show |
8 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.-156-1262A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48327299 | |||||||
| chr2:48327451 | CT | C | 100 | a0001c0001t0001g0159 a0001c0001t0001g0214 a0001c0001t0001g0231 others(97): Show |
102 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.-156-1099delT | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48327451 | ||||||
| chr2:48327615 | T | G | 5 | a0001c0001t0001g0098 a0001c0001t0001g0150 a0001c0001t0001g0165 others(2): Show |
5 | HG00733.hp1 HG01981.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.-156-946T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48327615 | |||||||
| chr2:48327645 | G | A | 159 | a0001c0001t0001g0159 a0001c0001t0001g0213 a0001c0001t0001g0214 others(156): Show |
165 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.-156-916G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48327645 | |||||||
| chr2:48327688 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-156-873A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48327688 | |||||||
| chr2:48327816 | G | A | 5 | a0001c0001t0001g0049 a0001c0001t0001g0106 a0001c0001t0001g0166 others(2): Show |
5 | HG00639.hp1 HG01123.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.-156-745G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48327816 | |||||||
| chr2:48328056 | A | G | 2 | a0001c0001t0001g0152 a0001c0001t0024g0202 |
2 | HG01243.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-156-505A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48328056 | |||||||
| chr2:48328153 | G | A | 9 | a0001c0001t0001g0012 a0001c0001t0001g0102 a0001c0001t0001g0103 others(6): Show |
9 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(6): Show |
intron_variant | MODIFIER | c.-156-408G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48328153 | |||||||
| chr2:48328338 | C | G | 129 | a0001c0001t0001g0159 a0001c0001t0001g0213 a0001c0001t0001g0214 others(126): Show |
131 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.-156-223C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48328338 | |||||||
| chr2:48328446 | A | G | 11 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0003 others(8): Show |
13 | HG01433.hp2 HG01891.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.-156-115A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48328446 | |||||||
| chr2:48328482 | C | T | 109 | a0001c0001t0001g0159 a0001c0001t0001g0214 a0001c0001t0001g0231 others(106): Show |
111 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.-156-79C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48328482 | |||||||
| chr2:48328485 | C | A | 12 | a0001c0002t0003g0015 a0001c0002t0003g0091 a0001c0002t0003g0246 others(9): Show |
12 | HG00738.hp2 HG01109.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-156-76C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48328485 | |||||||
| chr2:48328744 | G | A | 1 | a0001c0001t0001g0072 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-15+42G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48328744 | |||||||
| chr2:48328758 | C | A | 30 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0022 others(27): Show |
34 | HG01069.hp1 HG01123.hp1 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.-15+56C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48328758 | |||||||
| chr2:48328786 | T | C | 1 | a0001c0003t0001g0148 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-15+84T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48328786 | |||||||
| chr2:48328857 | G | T | 14 | a0001c0002t0003g0015 a0001c0002t0003g0091 a0001c0002t0003g0246 others(11): Show |
14 | HG00738.hp2 HG01109.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.-15+155G>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48328857 | |||||||
| chr2:48329167 | G | A | 1 | a0001c0001t0002g0035 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-15+465G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48329167 | |||||||
| chr2:48329231 | G | A | 1 | a0001c0001t0001g0221 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-15+529G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48329231 | |||||||
| chr2:48329343 | A | G | 166 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(163): Show |
172 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.-15+641A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48329343 | |||||||
| chr2:48329550 | G | A | 87 | a0001c0001t0001g0159 a0001c0001t0001g0214 a0001c0001t0001g0231 others(84): Show |
89 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.-15+848G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48329550 | |||||||
| chr2:48329616 | A | C | 3 | a0001c0001t0001g0071 a0001c0001t0001g0075 a0001c0001t0001g0085 |
3 | NA18612.hp1 NA18994.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.-15+914A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48329616 | |||||||
| chr2:48329748 | A | T | 1 | a0001c0001t0001g0075 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-15+1046A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48329748 | |||||||
| chr2:48329755 | T | C | 3 | a0001c0001t0001g0012 a0001c0001t0001g0102 a0001c0001t0001g0103 |
3 | HG00099.hp2 HG00642.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-15+1053T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48329755 | |||||||
| chr2:48329831 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-15+1129A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48329831 | |||||||
| chr2:48329846 | C | T | 287 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0014 others(284): Show |
294 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.-15+1144C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48329846 | |||||||
| chr2:48330033 | G | A | 1 | a0001c0002t0002g0266 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-15+1331G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48330033 | |||||||
| chr2:48330037 | C | A | 1 | a0001c0003t0016g0135 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-15+1335C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48330037 | |||||||
| chr2:48330608 | G | C | 3 | a0001c0002t0003g0015 a0001c0002t0003g0256 a0001c0002t0003g0257 |
3 | HG02717.hp2 HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-15+1906G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48330608 | |||||||
| chr2:48330631 | G | A | 1 | a0001c0002t0002g0267 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-15+1929G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48330631 | |||||||
| chr2:48330657 | T | G | 1 | a0001c0001t0001g0076 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-15+1955T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48330657 | |||||||
| chr2:48330732 | C | T | 21 | a0001c0001t0001g0213 a0001c0001t0001g0215 a0001c0001t0001g0216 others(18): Show |
21 | HG00099.hp1 HG00438.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.-15+2030C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48330732 | |||||||
| chr2:48330756 | CTTAAA | C | 21 | a0001c0001t0001g0213 a0001c0001t0001g0215 a0001c0001t0001g0216 others(18): Show |
21 | HG00099.hp1 HG00438.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.-15+2059_-15+2063d others(7): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48330756 | ||||||
| chr2:48330791 | C | T | 158 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(155): Show |
164 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.-15+2089C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48330791 | |||||||
| chr2:48330947 | C | T | 159 | a0001c0001t0001g0200 a0001c0001t0001g0213 a0001c0001t0001g0214 others(156): Show |
165 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.-15+2245C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48330947 | |||||||
| chr2:48331077 | G | A | 1 | a0001c0002t0002g0295 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-15+2375G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48331077 | |||||||
| chr2:48331118 | A | G | 1 | a0001c0002t0002g0321 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-15+2416A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48331118 | |||||||
| chr2:48331121 | A | C | 33 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(30): Show |
37 | HG01069.hp1 HG01123.hp1 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.-15+2419A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48331121 | |||||||
| chr2:48331175 | C | T | 11 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0003 others(8): Show |
13 | HG01433.hp2 HG01891.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.-15+2473C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48331175 | |||||||
| chr2:48331311 | T | C | 33 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(30): Show |
37 | HG01069.hp1 HG01123.hp1 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.-15+2609T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48331311 | |||||||
| chr2:48331343 | CTATAG | C | 8 | a0001c0002t0006g0237 a0001c0002t0006g0239 a0001c0002t0006g0240 others(5): Show |
8 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.-15+2647_-15+2651d others(7): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48331343 | ||||||
| chr2:48331356 | A | G | 2 | a0001c0003t0007g0010 a0001c0003t0007g0011 |
2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-15+2654A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48331356 | |||||||
| chr2:48331452 | G | A | 21 | a0001c0001t0001g0213 a0001c0001t0001g0215 a0001c0001t0001g0216 others(18): Show |
21 | HG00099.hp1 HG00438.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.-15+2750G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48331452 | |||||||
| chr2:48331458 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-15+2756A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48331458 | |||||||
| chr2:48331480 | T | G | 86 | a0001c0001t0001g0214 a0001c0001t0001g0231 a0001c0001t0001g0323 others(83): Show |
88 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.-15+2778T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48331480 | |||||||
| chr2:48331545 | C | G | 86 | a0001c0001t0001g0214 a0001c0001t0001g0231 a0001c0001t0001g0323 others(83): Show |
88 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.-15+2843C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48331545 | |||||||
| chr2:48331631 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-15+2929A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48331631 | |||||||
| chr2:48331732 | G | A | 1 | a0001c0003t0001g0136 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-15+3030G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48331732 | |||||||
| chr2:48331792 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-15+3090C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48331792 | |||||||
| chr2:48331991 | A | G | 1 | a0001c0001t0001g0213 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-15+3289A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48331991 | |||||||
| chr2:48332408 | A | G | 1 | a0001c0002t0002g0260 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-15+3706A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48332408 | |||||||
| chr2:48332580 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-15+3878A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48332580 | |||||||
| chr2:48332722 | T | C | 165 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(162): Show |
171 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.-15+4020T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48332722 | |||||||
| chr2:48332913 | C | A | 30 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0022 others(27): Show |
34 | HG01069.hp1 HG01123.hp1 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.-15+4211C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48332913 | |||||||
| chr2:48332981 | A | G | 1 | a0001c0001t0001g0224 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-15+4279A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48332981 | |||||||
| chr2:48332997 | A | AT | 123 | a0001c0001t0001g0129 a0001c0001t0001g0203 a0001c0001t0001g0213 others(120): Show |
125 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.-15+4300dupT | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48332997 | ||||||
| chr2:48333088 | T | G | 1 | a0001c0002t0002g0290 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-15+4386T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48333088 | |||||||
| chr2:48333094 | T | C | 30 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0022 others(27): Show |
34 | HG01069.hp1 HG01123.hp1 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.-15+4392T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48333094 | |||||||
| chr2:48333222 | A | T | 2 | a0001c0001t0001g0051 a0001c0001t0001g0052 |
2 | HG03704.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-15+4520A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48333222 | |||||||
| chr2:48333246 | A | G | 1 | a0001c0002t0002g0294 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-15+4544A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48333246 | |||||||
| chr2:48333252 | TATCTCTT others(4): Show |
T | 1 | a0001c0001t0002g0038 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-15+4558_-15+4568d others(13): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48333252 | ||||||
| chr2:48333263 | C | T | 1 | a0001c0002t0002g0294 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-15+4561C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48333263 | |||||||
| chr2:48333406 | A | G | 86 | a0001c0001t0001g0214 a0001c0001t0001g0231 a0001c0001t0001g0323 others(83): Show |
88 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.-15+4704A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48333406 | |||||||
| chr2:48333535 | G | C | 1 | a0001c0001t0001g0108 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-15+4833G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48333535 | |||||||
| chr2:48333640 | A | G | 1 | a0001c0001t0001g0108 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-15+4938A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48333640 | |||||||
| chr2:48333848 | G | C | 150 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(147): Show |
156 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.-15+5146G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48333848 | |||||||
| chr2:48333888 | G | GGT | 4 | a0001c0002t0002g0293 a0001c0002t0002g0302 a0001c0002t0002g0303 others(1): Show |
4 | HG00558.hp2 HG01952.hp2 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+5203_-15+5204d others(4): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48333888 | ||||||
| chr2:48334074 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-15+5372A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48334074 | |||||||
| chr2:48334095 | G | C | 1 | a0001c0001t0001g0057 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-15+5393G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48334095 | |||||||
| chr2:48334171 | T | C | 1 | a0001c0001t0001g0236 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-15+5469T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48334171 | |||||||
| chr2:48334307 | T | A | 9 | a0001c0001t0001g0007 a0001c0001t0001g0050 a0001c0001t0001g0144 others(6): Show |
10 | HG02109.hp2 HG02280.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-15+5605T>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48334307 | |||||||
| chr2:48334482 | ATC | A | 107 | a0001c0001t0001g0214 a0001c0001t0001g0231 a0001c0002t0002g0008 others(104): Show |
109 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.-15+5782_-15+5783d others(4): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48334482 | ||||||
| chr2:48334605 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-15+5903C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48334605 | |||||||
| chr2:48334709 | C | T | 45 | a0001c0001t0001g0013 a0001c0001t0001g0054 a0001c0001t0001g0056 others(42): Show |
48 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.-15+6007C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48334709 | |||||||
| chr2:48334736 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-15+6034C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48334736 | |||||||
| chr2:48334793 | A | T | 4 | a0001c0001t0001g0127 a0001c0001t0001g0152 a0001c0001t0001g0159 others(1): Show |
4 | HG01243.hp2 HG02886.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15+6091A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48334793 | |||||||
| chr2:48334829 | A | G | 4 | a0001c0001t0001g0070 a0001c0002t0002g0230 a0001c0002t0002g0317 others(1): Show |
4 | HG02056.hp1 NA18960.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+6127A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48334829 | |||||||
| chr2:48334857 | C | T | 8 | a0001c0002t0006g0237 a0001c0002t0006g0239 a0001c0002t0006g0240 others(5): Show |
8 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.-15+6155C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48334857 | |||||||
| chr2:48335021 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-15+6319C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48335021 | |||||||
| chr2:48335088 | A | G | 1 | a0001c0002t0002g0290 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-15+6386A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48335088 | |||||||
| chr2:48335161 | T | G | 1 | a0001c0001t0001g0187 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-15+6459T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48335161 | |||||||
| chr2:48335165 | G | A | 18 | a0001c0001t0001g0012 a0001c0001t0001g0099 a0001c0001t0001g0102 others(15): Show |
18 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.-15+6463G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48335165 | |||||||
| chr2:48335173 | A | G | 4 | a0001c0002t0006g0240 a0001c0002t0006g0242 a0001c0002t0006g0243 others(1): Show |
4 | HG00280.hp1 HG01081.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+6471A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48335173 | |||||||
| chr2:48335291 | A | C | 1 | a0001c0001t0002g0041 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-15+6589A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48335291 | |||||||
| chr2:48335334 | TG | T | 8 | a0001c0002t0006g0237 a0001c0002t0006g0239 a0001c0002t0006g0240 others(5): Show |
8 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.-15+6633delG | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48335334 | |||||||
| chr2:48335351 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-15+6649A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48335351 | |||||||
| chr2:48335526 | A | G | 1 | a0001c0001t0014g0160 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-15+6824A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48335526 | |||||||
| chr2:48335551 | A | AGCAAAAA others(18): Show |
161 | a0001c0001t0001g0129 a0001c0001t0001g0203 a0001c0001t0001g0213 others(158): Show |
167 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.-15+6859_-15+6860i others(27): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48335551 | ||||||
| chr2:48335593 | A | T | 1 | a0001c0001t0001g0179 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-15+6891A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48335593 | |||||||
| chr2:48335680 | T | C | 54 | a0001c0001t0001g0129 a0001c0001t0001g0203 a0001c0001t0001g0213 others(51): Show |
58 | HG00099.hp1 HG00438.hp2 HG01069.hp1 others(55): Show |
intron_variant | MODIFIER | c.-15+6978T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48335680 | |||||||
| chr2:48335803 | G | A | 3 | a0001c0002t0002g0268 a0001c0002t0002g0319 a0001c0002t0003g0091 |
3 | HG02080.hp2 HG03098.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.-15+7101G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48335803 | |||||||
| chr2:48335826 | G | C | 1 | a0001c0001t0001g0054 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-15+7124G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48335826 | |||||||
| chr2:48335915 | C | T | 3 | a0001c0002t0003g0250 a0001c0002t0003g0251 a0001c0002t0003g0252 |
3 | HG03225.hp2 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-15+7213C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48335915 | |||||||
| chr2:48335958 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-15+7256G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48335958 | |||||||
| chr2:48335958 | G | T | 1 | a0001c0002t0002g0316 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-15+7256G>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48335958 | |||||||
| chr2:48336006 | C | T | 1 | a0001c0002t0002g0295 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-15+7304C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336006 | |||||||
| chr2:48336033 | A | AT | 125 | a0001c0001t0001g0129 a0001c0001t0001g0203 a0001c0001t0001g0213 others(122): Show |
127 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.-15+7331_-15+7332i others(3): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336033 | |||||||
| chr2:48336036 | A | AT | 8 | a0001c0002t0006g0237 a0001c0002t0006g0239 a0001c0002t0006g0240 others(5): Show |
8 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.-15+7334_-15+7335i others(3): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336036 | |||||||
| chr2:48336036 | A | T | 125 | a0001c0001t0001g0129 a0001c0001t0001g0203 a0001c0001t0001g0213 others(122): Show |
127 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.-15+7334A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336036 | |||||||
| chr2:48336039 | A | T | 163 | a0001c0001t0001g0129 a0001c0001t0001g0203 a0001c0001t0001g0213 others(160): Show |
169 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.-15+7337A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336039 | |||||||
| chr2:48336131 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-15+7429C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336131 | |||||||
| chr2:48336142 | G | A | 3 | a0001c0002t0003g0015 a0001c0002t0003g0256 a0001c0002t0003g0257 |
3 | HG02717.hp2 HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-15+7440G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336142 | |||||||
| chr2:48336202 | A | G | 159 | a0001c0001t0001g0129 a0001c0001t0001g0203 a0001c0001t0001g0213 others(156): Show |
165 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.-15+7500A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336202 | |||||||
| chr2:48336202 | A | T | 3 | a0001c0002t0003g0015 a0001c0002t0003g0256 a0001c0002t0003g0257 |
3 | HG02717.hp2 HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-15+7500A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336202 | |||||||
| chr2:48336225 | G | GA | 10 | a0001c0001t0001g0007 a0001c0001t0001g0050 a0001c0001t0001g0144 others(7): Show |
11 | HG02109.hp2 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-15+7526dupA | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48336225 | ||||||
| chr2:48336347 | G | T | 5 | a0001c0001t0001g0219 a0001c0001t0001g0225 a0001c0001t0001g0227 others(2): Show |
5 | HG01358.hp1 HG02683.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.-15+7645G>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336347 | |||||||
| chr2:48336408 | C | CAA | 9 | a0001c0002t0002g0258 a0001c0002t0002g0283 a0001c0002t0002g0284 others(6): Show |
9 | HG03710.hp2 NA18972.hp2 NA18990.hp1 others(6): Show |
intron_variant | MODIFIER | c.-15+7716_-15+7717d others(4): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48336408 | ||||||
| chr2:48336408 | C | CAAAA | 50 | a0001c0001t0001g0129 a0001c0001t0001g0203 a0001c0001t0001g0213 others(47): Show |
54 | HG00099.hp1 HG00438.hp2 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.-15+7714_-15+7717d others(6): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48336408 | ||||||
| chr2:48336418 | A | AAAAT | 88 | a0001c0001t0001g0323 a0001c0001t0002g0032 a0001c0001t0002g0042 others(85): Show |
90 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.-15+7717_-15+7718i others(6): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48336418 | ||||||
| chr2:48336418 | A | T | 2 | a0001c0001t0001g0070 a0001c0001t0001g0124 |
2 | NA19074.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-15+7716A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336418 | |||||||
| chr2:48336420 | T | A | 6 | a0001c0001t0001g0214 a0001c0001t0001g0231 a0001c0001t0002g0039 others(3): Show |
6 | HG01257.hp1 HG02602.hp2 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15+7718T>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336420 | |||||||
| chr2:48336431 | G | A | 16 | a0001c0001t0001g0214 a0001c0001t0001g0231 a0001c0002t0002g0258 others(13): Show |
16 | HG01257.hp1 HG02055.hp1 HG02602.hp2 others(13): Show |
intron_variant | MODIFIER | c.-15+7729G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336431 | |||||||
| chr2:48336433 | A | G | 9 | a0001c0002t0002g0258 a0001c0002t0002g0283 a0001c0002t0002g0284 others(6): Show |
9 | HG03710.hp2 NA18972.hp2 NA18990.hp1 others(6): Show |
intron_variant | MODIFIER | c.-15+7731A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336433 | |||||||
| chr2:48336433 | ATATGTG | A | 4 | a0001c0001t0001g0214 a0001c0001t0001g0231 a0001c0002t0002g0288 others(1): Show |
4 | HG02602.hp2 HG03492.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+7733_-15+7738d others(8): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48336433 | ||||||
| chr2:48336435 | A | ATG | 44 | a0001c0001t0001g0052 a0001c0001t0001g0098 a0001c0001t0001g0101 others(41): Show |
44 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.-15+7755_-15+7756d others(4): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48336435 | ||||||
| chr2:48336435 | A | ATGTG | 5 | a0001c0002t0003g0246 a0001c0002t0003g0248 a0001c0002t0003g0249 others(2): Show |
5 | HG00738.hp2 HG01109.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15+7753_-15+7756d others(6): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48336435 | ||||||
| chr2:48336435 | A | G | 1 | a0001c0002t0006g0239 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-15+7733A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336435 | |||||||
| chr2:48336437 | G | A | 12 | a0001c0002t0002g0258 a0001c0002t0002g0283 a0001c0002t0002g0284 others(9): Show |
12 | HG01257.hp1 HG02055.hp1 HG03098.hp2 others(9): Show |
intron_variant | MODIFIER | c.-15+7735G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336437 | |||||||
| chr2:48336439 | G | A | 2 | a0001c0001t0002g0039 a0001c0002t0006g0239 |
2 | HG01257.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.-15+7737G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336439 | |||||||
| chr2:48336441 | G | A | 1 | a0001c0001t0002g0039 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-15+7739G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336441 | |||||||
| chr2:48336443 | G | A | 4 | a0001c0001t0001g0214 a0001c0001t0001g0231 a0001c0002t0002g0288 others(1): Show |
4 | HG02602.hp2 HG03492.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+7741G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336443 | |||||||
| chr2:48336445 | G | A | 4 | a0001c0001t0001g0214 a0001c0001t0001g0231 a0001c0002t0002g0288 others(1): Show |
4 | HG02602.hp2 HG03492.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+7743G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336445 | |||||||
| chr2:48336457 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-15+7755G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336457 | |||||||
| chr2:48336457 | GTA | G | 19 | a0001c0001t0001g0225 a0001c0001t0002g0022 a0001c0001t0005g0002 others(16): Show |
21 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.-15+7763_-15+7764d others(4): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48336457 | ||||||
| chr2:48336459 | A | G | 45 | a0001c0001t0001g0103 a0001c0001t0001g0119 a0001c0001t0001g0129 others(42): Show |
47 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.-15+7757A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336459 | |||||||
| chr2:48336567 | C | G | 1 | a0001c0001t0021g0033 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-15+7865C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336567 | |||||||
| chr2:48336571 | C | T | 101 | a0001c0001t0001g0214 a0001c0001t0001g0231 a0001c0001t0001g0323 others(98): Show |
103 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.-15+7869C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336571 | |||||||
| chr2:48336702 | T | C | 163 | a0001c0001t0001g0129 a0001c0001t0001g0203 a0001c0001t0001g0213 others(160): Show |
169 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.-15+8000T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336702 | |||||||
| chr2:48336861 | C | T | 5 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0068 others(2): Show |
5 | HG02080.hp1 NA18949.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.-15+8159C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336861 | |||||||
| chr2:48336956 | A | G | 1 | a0001c0001t0001g0070 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-15+8254A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336956 | |||||||
| chr2:48337055 | CT | C | 116 | a0001c0001t0001g0050 a0001c0001t0001g0058 a0001c0001t0001g0078 others(113): Show |
118 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.-15+8367delT | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48337055 | ||||||
| chr2:48337291 | C | CT | 53 | a0001c0001t0001g0079 a0001c0001t0001g0197 a0001c0001t0001g0213 others(50): Show |
57 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.-15+8605dupT | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48337291 | ||||||
| chr2:48337319 | G | A | 1 | a0001c0002t0006g0242 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-15+8617G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48337319 | |||||||
| chr2:48337420 | C | G | 2 | a0001c0001t0001g0229 a0001c0001t0001g0233 |
2 | HG00099.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.-15+8718C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48337420 | |||||||
| chr2:48337623 | G | A | 2 | a0001c0002t0003g0248 a0001c0002t0003g0249 |
2 | HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-14-8578G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48337623 | |||||||
| chr2:48337648 | C | A | 2 | a0001c0001t0002g0030 a0001c0001t0002g0034 |
2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-14-8553C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48337648 | |||||||
| chr2:48337686 | A | G | 1 | a0001c0001t0024g0202 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-14-8515A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48337686 | |||||||
| chr2:48337859 | T | A | 50 | a0001c0001t0001g0129 a0001c0001t0001g0203 a0001c0001t0001g0213 others(47): Show |
54 | HG00099.hp1 HG00438.hp2 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.-14-8342T>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48337859 | |||||||
| chr2:48337866 | G | A | 160 | a0001c0001t0001g0129 a0001c0001t0001g0203 a0001c0001t0001g0213 others(157): Show |
166 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.-14-8335G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48337866 | |||||||
| chr2:48338080 | A | G | 2 | a0001c0003t0007g0010 a0001c0003t0007g0011 |
2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-14-8121A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48338080 | |||||||
| chr2:48338141 | A | G | 3 | a0001c0002t0003g0015 a0001c0002t0003g0256 a0001c0002t0003g0257 |
3 | HG02717.hp2 HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-14-8060A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48338141 | |||||||
| chr2:48338196 | G | A | 161 | a0001c0001t0001g0129 a0001c0001t0001g0203 a0001c0001t0001g0213 others(158): Show |
167 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.-14-8005G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48338196 | |||||||
| chr2:48338203 | C | A | 1 | a0001c0001t0001g0012 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-14-7998C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48338203 | |||||||
| chr2:48338238 | T | G | 1 | a0001c0001t0005g0029 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-14-7963T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48338238 | |||||||
| chr2:48338385 | C | A | 11 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0003 others(8): Show |
13 | HG01433.hp2 HG01891.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.-14-7816C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48338385 | |||||||
| chr2:48338386 | A | T | 11 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0003 others(8): Show |
13 | HG01433.hp2 HG01891.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.-14-7815A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48338386 | |||||||
| chr2:48338396 | C | A | 161 | a0001c0001t0001g0129 a0001c0001t0001g0203 a0001c0001t0001g0213 others(158): Show |
167 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.-14-7805C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48338396 | |||||||
| chr2:48338398 | A | AT | 160 | a0001c0001t0001g0054 a0001c0001t0001g0129 a0001c0001t0001g0203 others(157): Show |
166 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.-14-7790dupT | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48338398 | ||||||
| chr2:48338555 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-14-7646C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48338555 | |||||||
| chr2:48338643 | C | T | 130 | a0001c0001t0001g0129 a0001c0001t0001g0203 a0001c0001t0001g0213 others(127): Show |
132 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.-14-7558C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48338643 | |||||||
| chr2:48338840 | A | G | 2 | a0001c0002t0002g0268 a0001c0002t0002g0319 |
2 | HG02080.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.-14-7361A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48338840 | |||||||
| chr2:48338892 | C | T | 212 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0050 others(209): Show |
219 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.-14-7309C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48338892 | |||||||
| chr2:48339073 | T | C | 3 | a0001c0001t0001g0152 a0001c0001t0001g0159 a0001c0001t0024g0202 |
3 | HG01243.hp2 HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-14-7128T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48339073 | |||||||
| chr2:48339277 | C | G | 30 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0022 others(27): Show |
34 | HG01069.hp1 HG01123.hp1 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.-14-6924C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48339277 | |||||||
| chr2:48339796 | C | T | 159 | a0001c0001t0001g0129 a0001c0001t0001g0203 a0001c0001t0001g0213 others(156): Show |
165 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.-14-6405C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48339796 | |||||||
| chr2:48339799 | A | G | 159 | a0001c0001t0001g0129 a0001c0001t0001g0203 a0001c0001t0001g0213 others(156): Show |
165 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.-14-6402A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48339799 | |||||||
| chr2:48339887 | A | G | 2 | a0001c0001t0001g0214 a0001c0001t0001g0231 |
2 | HG02602.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-14-6314A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48339887 | |||||||
| chr2:48340305 | T | C | 10 | a0001c0001t0001g0007 a0001c0001t0001g0050 a0001c0001t0001g0144 others(7): Show |
11 | HG02109.hp2 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-14-5896T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48340305 | |||||||
| chr2:48340468 | G | A | 1 | a0001c0001t0001g0172 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-14-5733G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48340468 | |||||||
| chr2:48340545 | G | A | 1 | a0001c0001t0001g0209 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-14-5656G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48340545 | |||||||
| chr2:48340574 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-14-5627C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48340574 | |||||||
| chr2:48340666 | T | G | 2 | a0001c0003t0007g0010 a0001c0003t0007g0011 |
2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-14-5535T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48340666 | |||||||
| chr2:48340711 | G | A | 1 | a0001c0002t0003g0091 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-14-5490G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48340711 | |||||||
| chr2:48340825 | C | G | 53 | a0001c0001t0001g0129 a0001c0001t0001g0203 a0001c0001t0001g0213 others(50): Show |
57 | HG00099.hp1 HG00438.hp2 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.-14-5376C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48340825 | |||||||
| chr2:48340871 | C | A | 101 | a0001c0001t0001g0214 a0001c0001t0001g0231 a0001c0001t0001g0323 others(98): Show |
103 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.-14-5330C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48340871 | |||||||
| chr2:48340922 | A | G | 2 | a0001c0002t0002g0301 a0001c0002t0002g0315 |
2 | NA18990.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.-14-5279A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48340922 | |||||||
| chr2:48340944 | A | G | 2 | a0001c0001t0001g0095 a0001c0001t0001g0096 |
2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-14-5257A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48340944 | |||||||
| chr2:48340969 | C | T | 2 | a0001c0003t0007g0010 a0001c0003t0007g0011 |
2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-14-5232C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48340969 | |||||||
| chr2:48341226 | A | G | 124 | a0001c0001t0001g0129 a0001c0001t0001g0203 a0001c0001t0001g0213 others(121): Show |
126 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.-14-4975A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48341226 | |||||||
| chr2:48341441 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-14-4760A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48341441 | |||||||
| chr2:48341580 | G | A | 3 | a0001c0001t0001g0323 a0001c0002t0002g0269 a0001c0002t0002g0270 |
3 | HG02132.hp2 HG02135.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.-14-4621G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48341580 | |||||||
| chr2:48341726 | G | A | 161 | a0001c0001t0001g0129 a0001c0001t0001g0203 a0001c0001t0001g0213 others(158): Show |
167 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.-14-4475G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48341726 | |||||||
| chr2:48341766 | G | T | 30 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0022 others(27): Show |
34 | HG01069.hp1 HG01123.hp1 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.-14-4435G>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48341766 | |||||||
| chr2:48341920 | A | G | 162 | a0001c0001t0001g0129 a0001c0001t0001g0203 a0001c0001t0001g0213 others(159): Show |
168 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.-14-4281A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48341920 | |||||||
| chr2:48342047 | A | T | 19 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0030 others(16): Show |
21 | HG01069.hp1 HG01123.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.-14-4154A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48342047 | |||||||
| chr2:48342176 | A | G | 8 | a0001c0002t0006g0237 a0001c0002t0006g0239 a0001c0002t0006g0240 others(5): Show |
8 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.-14-4025A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48342176 | |||||||
| chr2:48342396 | AG | A | 29 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0022 others(26): Show |
33 | HG01069.hp1 HG01123.hp1 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.-14-3802delG | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48342396 | ||||||
| chr2:48342443 | A | G | 31 | a0001c0001t0001g0014 a0001c0001t0001g0051 a0001c0001t0001g0052 others(28): Show |
31 | HG00642.hp1 HG00733.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.-14-3758A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48342443 | |||||||
| chr2:48342503 | T | G | 3 | a0001c0002t0002g0267 a0001c0002t0002g0316 a0001c0002t0002g0325 |
3 | NA18994.hp2 NA19005.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.-14-3698T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48342503 | |||||||
| chr2:48342518 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-14-3683G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48342518 | |||||||
| chr2:48342553 | T | A | 1 | a0001c0002t0003g0015 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-14-3648T>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48342553 | |||||||
| chr2:48342728 | A | G | 1 | a0001c0001t0001g0255 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-14-3473A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48342728 | |||||||
| chr2:48342732 | G | A | 2 | a0001c0003t0007g0010 a0001c0003t0007g0011 |
2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-14-3469G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48342732 | |||||||
| chr2:48342765 | T | G | 2 | a0001c0002t0006g0240 a0001c0002t0006g0244 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-14-3436T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48342765 | |||||||
| chr2:48342818 | A | G | 2 | a0001c0001t0001g0229 a0001c0001t0001g0233 |
2 | HG00099.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.-14-3383A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48342818 | |||||||
| chr2:48342997 | A | C | 4 | a0001c0003t0001g0136 a0001c0003t0001g0137 a0001c0003t0001g0148 others(1): Show |
4 | HG02109.hp1 HG02451.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14-3204A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48342997 | |||||||
| chr2:48343109 | T | G | 1 | a0001c0004t0002g0021 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-14-3092T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48343109 | |||||||
| chr2:48343161 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-14-3040C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48343161 | |||||||
| chr2:48343180 | C | T | 2 | a0001c0002t0002g0282 a0001c0002t0002g0313 |
2 | HG00621.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.-14-3021C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48343180 | |||||||
| chr2:48343239 | T | A | 1 | a0001c0001t0001g0124 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-14-2962T>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48343239 | |||||||
| chr2:48343369 | G | T | 130 | a0001c0001t0001g0129 a0001c0001t0001g0203 a0001c0001t0001g0213 others(127): Show |
132 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.-14-2832G>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48343369 | |||||||
| chr2:48343761 | T | TA | 32 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0022 others(29): Show |
36 | HG01069.hp1 HG01123.hp1 HG01192.hp2 others(33): Show |
intron_variant | MODIFIER | c.-14-2427dupA | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48343761 | ||||||
| chr2:48343937 | T | G | 1 | a0001c0002t0006g0243 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-14-2264T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48343937 | |||||||
| chr2:48343940 | A | G | 2 | a0001c0001t0001g0067 a0001c0001t0001g0084 |
2 | NA18941.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.-14-2261A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48343940 | |||||||
| chr2:48343950 | T | A | 1 | a0001c0004t0002g0021 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-14-2251T>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48343950 | |||||||
| chr2:48344040 | C | T | 1 | a0001c0001t0002g0039 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-14-2161C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48344040 | |||||||
| chr2:48344044 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-14-2157A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48344044 | |||||||
| chr2:48344072 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-14-2129G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48344072 | |||||||
| chr2:48344277 | C | T | 122 | a0001c0001t0001g0129 a0001c0001t0001g0203 a0001c0001t0001g0213 others(119): Show |
124 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.-14-1924C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48344277 | |||||||
| chr2:48344497 | C | T | 30 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0022 others(27): Show |
34 | HG01069.hp1 HG01123.hp1 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.-14-1704C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48344497 | |||||||
| chr2:48344685 | A | T | 30 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0022 others(27): Show |
34 | HG01069.hp1 HG01123.hp1 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.-14-1516A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48344685 | |||||||
| chr2:48344712 | T | A | 89 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0220 others(86): Show |
91 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.-14-1489T>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48344712 | |||||||
| chr2:48344778 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-14-1423G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48344778 | |||||||
| chr2:48344779 | G | T | 1 | a0001c0001t0001g0139 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-14-1422G>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48344779 | |||||||
| chr2:48344840 | A | AC | 39 | a0001c0001t0001g0079 a0001c0001t0001g0085 a0001c0001t0001g0089 others(36): Show |
40 | HG00099.hp2 HG00621.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.-14-1349dupC | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48344840 | ||||||
| chr2:48344840 | A | ACC | 19 | a0001c0001t0001g0012 a0001c0001t0001g0053 a0001c0001t0001g0058 others(16): Show |
19 | HG00642.hp2 HG01081.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.-14-1350_-14-1349d others(4): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48344840 | ||||||
| chr2:48344840 | AC | A | 42 | a0001c0001t0001g0070 a0001c0001t0001g0092 a0001c0001t0001g0115 others(39): Show |
46 | HG00408.hp2 HG00738.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.-14-1349delC | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48344840 | ||||||
| chr2:48344840 | ACC | A | 99 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0220 others(96): Show |
101 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.-14-1350_-14-1349d others(4): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48344840 | ||||||
| chr2:48344840 | ACCC | A | 20 | a0001c0001t0001g0129 a0001c0001t0001g0203 a0001c0001t0001g0213 others(17): Show |
20 | HG00099.hp1 HG00438.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.-14-1351_-14-1349d others(5): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48344840 | ||||||
| chr2:48345201 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-14-1000T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48345201 | |||||||
| chr2:48345278 | T | C | 132 | a0001c0001t0001g0129 a0001c0001t0001g0203 a0001c0001t0001g0213 others(129): Show |
134 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.-14-923T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48345278 | |||||||
| chr2:48345361 | G | C | 21 | a0001c0001t0001g0129 a0001c0001t0001g0203 a0001c0001t0001g0213 others(18): Show |
21 | HG00099.hp1 HG00438.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.-14-840G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48345361 | |||||||
| chr2:48345514 | T | G | 35 | a0001c0001t0001g0129 a0001c0001t0001g0203 a0001c0001t0001g0213 others(32): Show |
35 | HG00099.hp1 HG00438.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.-14-687T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48345514 | |||||||
| chr2:48345581 | A | G | 30 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0022 others(27): Show |
34 | HG01069.hp1 HG01123.hp1 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.-14-620A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48345581 | |||||||
| chr2:48345683 | A | C | 132 | a0001c0001t0001g0129 a0001c0001t0001g0203 a0001c0001t0001g0213 others(129): Show |
134 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.-14-518A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48345683 | |||||||
| chr2:48345770 | A | G | 132 | a0001c0001t0001g0129 a0001c0001t0001g0203 a0001c0001t0001g0213 others(129): Show |
134 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.-14-431A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48345770 | |||||||
| chr2:48345842 | A | G | 2 | a0001c0001t0001g0233 a0001c0002t0002g0270 |
2 | HG00099.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.-14-359A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48345842 | |||||||
| chr2:48345909 | G | A | 30 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0022 others(27): Show |
34 | HG01069.hp1 HG01123.hp1 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.-14-292G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48345909 | |||||||
| chr2:48345936 | A | G | 4 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0187 others(1): Show |
4 | HG02683.hp2 HG03669.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-265A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48345936 | |||||||
| chr2:48346062 | C | G | 1 | a0001c0001t0018g0105 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-14-139C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48346062 | |||||||
| chr2:48346145 | T | C | 1 | a0001c0004t0003g0043 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-14-56T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48346145 | |||||||
| chr2:48346756 | G | C | 10 | a0001c0001t0001g0049 a0001c0001t0001g0106 a0001c0001t0001g0141 others(7): Show |
10 | HG00639.hp1 HG01123.hp2 HG01346.hp1 others(7): Show |
splice_region_variant&intron_variant | LOW | c.537+5G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48346756 | |||||||
| chr2:48346767 | C | T | 6 | a0001c0003t0001g0133 a0001c0003t0001g0134 a0001c0003t0001g0136 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.537+16C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48346767 | |||||||
| chr2:48346845 | T | G | 1 | a0001c0001t0001g0222 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.537+94T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48346845 | |||||||
| chr2:48346896 | C | G | 1 | a0001c0002t0002g0260 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.537+145C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48346896 | |||||||
| chr2:48347025 | T | C | 135 | a0001c0001t0001g0013 a0001c0001t0001g0068 a0001c0001t0001g0089 others(132): Show |
137 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.537+274T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48347025 | |||||||
| chr2:48347172 | C | A | 2 | a0001c0001t0002g0030 a0001c0001t0002g0034 |
2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.537+421C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48347172 | |||||||
| chr2:48347187 | G | T | 2 | a0001c0001t0002g0030 a0001c0001t0002g0034 |
2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.537+436G>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48347187 | |||||||
| chr2:48347220 | C | CT | 70 | a0001c0001t0001g0049 a0001c0001t0001g0056 a0001c0001t0001g0069 others(67): Show |
71 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.537+493dupT | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48347220 | ||||||
| chr2:48347220 | C | CTT | 23 | a0001c0001t0001g0129 a0001c0001t0001g0203 a0001c0001t0001g0216 others(20): Show |
23 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(20): Show |
intron_variant | MODIFIER | c.537+492_537+493dup others(2): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48347220 | ||||||
| chr2:48347220 | C | CTTT | 7 | a0001c0001t0001g0213 a0001c0001t0001g0223 a0001c0001t0001g0224 others(4): Show |
7 | HG01358.hp1 HG02056.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.537+491_537+493dup others(3): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48347220 | ||||||
| chr2:48347220 | CT | C | 31 | a0001c0001t0001g0130 a0001c0001t0001g0204 a0001c0001t0002g0016 others(28): Show |
35 | HG00738.hp1 HG01069.hp1 HG01123.hp1 others(32): Show |
intron_variant | MODIFIER | c.537+493delT | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48347220 | ||||||
| chr2:48347232 | T | G | 19 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0030 others(16): Show |
21 | HG01069.hp1 HG01123.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.537+481T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48347232 | |||||||
| chr2:48347253 | G | A | 1 | a0001c0002t0002g0266 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.537+502G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48347253 | |||||||
| chr2:48347288 | G | C | 1 | a0001c0001t0001g0139 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.537+537G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48347288 | |||||||
| chr2:48347290 | G | A | 8 | a0001c0002t0006g0237 a0001c0002t0006g0239 a0001c0002t0006g0240 others(5): Show |
8 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.537+539G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48347290 | |||||||
| chr2:48347352 | A | C | 1 | a0001c0002t0002g0265 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.537+601A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48347352 | |||||||
| chr2:48347381 | C | T | 30 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0022 others(27): Show |
34 | HG01069.hp1 HG01123.hp1 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.537+630C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48347381 | |||||||
| chr2:48347533 | T | TTG | 21 | a0001c0001t0001g0050 a0001c0001t0001g0107 a0001c0001t0001g0108 others(18): Show |
21 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(18): Show |
intron_variant | MODIFIER | c.537+808_537+809dup others(2): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48347533 | ||||||
| chr2:48347533 | T | TTGTG | 28 | a0001c0001t0001g0129 a0001c0001t0001g0203 a0001c0001t0001g0213 others(25): Show |
28 | HG00099.hp1 HG00438.hp2 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.537+806_537+809dup others(4): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48347533 | ||||||
| chr2:48347533 | T | TTGTGTG | 91 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0220 others(88): Show |
93 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.537+804_537+809dup others(6): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48347533 | ||||||
| chr2:48347533 | T | TTGTGTGT others(1): Show |
7 | a0001c0002t0002g0266 a0001c0002t0002g0296 a0001c0002t0002g0319 others(4): Show |
7 | HG01106.hp2 HG01109.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.537+802_537+809dup others(8): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48347533 | ||||||
| chr2:48347902 | T | C | 2 | a0001c0002t0002g0265 a0001c0002t0002g0291 |
2 | NA18954.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.537+1151T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48347902 | |||||||
| chr2:48347936 | T | A | 1 | a0001c0002t0002g0289 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.537+1185T>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48347936 | |||||||
| chr2:48348236 | C | T | 1 | a0001c0002t0002g0264 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.537+1485C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48348236 | |||||||
| chr2:48348346 | A | C | 8 | a0001c0002t0006g0237 a0001c0002t0006g0239 a0001c0002t0006g0240 others(5): Show |
8 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.537+1595A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48348346 | |||||||
| chr2:48348427 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.537+1676A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48348427 | |||||||
| chr2:48348523 | A | T | 161 | a0001c0001t0001g0129 a0001c0001t0001g0203 a0001c0001t0001g0213 others(158): Show |
167 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.537+1772A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48348523 | |||||||
| chr2:48348559 | G | A | 88 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0220 others(85): Show |
90 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.537+1808G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48348559 | |||||||
| chr2:48348628 | G | C | 102 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0220 others(99): Show |
104 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.537+1877G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48348628 | |||||||
| chr2:48348636 | G | A | 30 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0022 others(27): Show |
34 | HG01069.hp1 HG01123.hp1 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.537+1885G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48348636 | |||||||
| chr2:48348649 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.537+1898T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48348649 | |||||||
| chr2:48348708 | C | G | 8 | a0001c0002t0006g0237 a0001c0002t0006g0239 a0001c0002t0006g0240 others(5): Show |
8 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.537+1957C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48348708 | |||||||
| chr2:48348760 | T | G | 1 | a0001c0001t0001g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.537+2009T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48348760 | |||||||
| chr2:48348785 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.537+2034A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48348785 | |||||||
| chr2:48348791 | G | C | 3 | a0001c0001t0001g0154 a0001c0001t0001g0157 a0001c0001t0001g0199 |
3 | HG02717.hp1 HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.537+2040G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48348791 | |||||||
| chr2:48349312 | C | T | 1 | a0001c0002t0006g0243 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.537+2561C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48349312 | |||||||
| chr2:48349324 | A | G | 6 | a0001c0001t0002g0016 a0001c0001t0002g0032 a0001c0001t0002g0038 others(3): Show |
6 | HG01069.hp1 HG02145.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.537+2573A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48349324 | |||||||
| chr2:48349409 | C | T | 107 | a0001c0001t0001g0214 a0001c0001t0001g0231 a0001c0001t0001g0323 others(104): Show |
109 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.537+2658C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48349409 | |||||||
| chr2:48349522 | C | T | 138 | a0001c0001t0001g0214 a0001c0001t0001g0231 a0001c0001t0001g0323 others(135): Show |
144 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.537+2771C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48349522 | |||||||
| chr2:48349548 | C | T | 108 | a0001c0001t0001g0214 a0001c0001t0001g0231 a0001c0001t0001g0323 others(105): Show |
110 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.537+2797C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48349548 | |||||||
| chr2:48349610 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.537+2859C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48349610 | |||||||
| chr2:48349681 | A | G | 5 | a0001c0001t0001g0104 a0001c0001t0001g0161 a0001c0001t0001g0164 others(2): Show |
5 | HG00639.hp2 HG01261.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.537+2930A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48349681 | |||||||
| chr2:48349830 | C | T | 1 | a0001c0001t0014g0160 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.537+3079C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48349830 | |||||||
| chr2:48349835 | A | G | 1 | a0001c0001t0014g0160 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.537+3084A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48349835 | |||||||
| chr2:48349840 | G | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0254 |
2 | HG00639.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.537+3089G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48349840 | |||||||
| chr2:48349964 | A | G | 100 | a0001c0001t0001g0214 a0001c0001t0001g0231 a0001c0001t0001g0323 others(97): Show |
102 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.537+3213A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48349964 | |||||||
| chr2:48350084 | G | C | 2 | a0001c0002t0003g0250 a0001c0002t0003g0251 |
2 | HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.537+3333G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48350084 | |||||||
| chr2:48350108 | A | T | 1 | a0001c0001t0001g0143 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.537+3357A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48350108 | |||||||
| chr2:48350664 | A | G | 2 | a0001c0001t0001g0214 a0001c0001t0001g0231 |
2 | HG02602.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.537+3913A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48350664 | |||||||
| chr2:48350758 | C | G | 2 | a0001c0001t0001g0229 a0001c0001t0001g0233 |
2 | HG00099.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.537+4007C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48350758 | |||||||
| chr2:48350987 | A | G | 1 | a0001c0001t0005g0002 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.537+4236A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48350987 | |||||||
| chr2:48351007 | C | T | 2 | a0001c0002t0002g0297 a0001c0002t0002g0311 |
2 | NA18991.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.537+4256C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48351007 | |||||||
| chr2:48351191 | G | A | 5 | a0001c0001t0001g0323 a0001c0002t0002g0265 a0001c0002t0002g0269 others(2): Show |
5 | HG02132.hp2 HG02135.hp1 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.537+4440G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48351191 | |||||||
| chr2:48351258 | G | A | 11 | a0001c0001t0001g0141 a0001c0001t0001g0156 a0001c0001t0001g0162 others(8): Show |
11 | HG02145.hp1 HG02809.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.537+4507G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48351258 | |||||||
| chr2:48351317 | G | T | 1 | a0001c0003t0001g0136 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.537+4566G>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48351317 | |||||||
| chr2:48351500 | G | A | 3 | a0001c0002t0003g0015 a0001c0002t0003g0256 a0001c0002t0003g0257 |
3 | HG02717.hp2 HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.537+4749G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48351500 | |||||||
| chr2:48351660 | G | A | 101 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0220 others(98): Show |
103 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.537+4909G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48351660 | |||||||
| chr2:48351783 | C | G | 1 | a0001c0002t0003g0091 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.537+5032C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48351783 | |||||||
| chr2:48352049 | T | TTTTGTGC others(8): Show |
1 | a0001c0002t0002g0303 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.537+5302_537+5303i others(17): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48352049 | ||||||
| chr2:48352055 | G | A | 1 | a0001c0002t0002g0303 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.537+5304G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48352055 | |||||||
| chr2:48352055 | G | GCTTCAGT others(8): Show |
108 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0220 others(105): Show |
110 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.537+5313_537+5327d others(17): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48352055 | ||||||
| chr2:48352220 | G | C | 11 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0003 others(8): Show |
13 | HG01433.hp2 HG01891.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.537+5469G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48352220 | |||||||
| chr2:48352303 | C | T | 2 | a0001c0001t0001g0229 a0001c0001t0001g0233 |
2 | HG00099.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.537+5552C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48352303 | |||||||
| chr2:48352332 | C | G | 4 | a0001c0001t0002g0030 a0001c0001t0002g0034 a0001c0001t0002g0039 others(1): Show |
4 | HG01884.hp1 HG01891.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.537+5581C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48352332 | |||||||
| chr2:48352585 | C | T | 2 | a0001c0001t0002g0030 a0001c0001t0002g0034 |
2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.537+5834C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48352585 | |||||||
| chr2:48352639 | G | A | 150 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(147): Show |
156 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.537+5888G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48352639 | |||||||
| chr2:48352647 | A | T | 8 | a0001c0002t0006g0237 a0001c0002t0006g0239 a0001c0002t0006g0240 others(5): Show |
8 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.537+5896A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48352647 | |||||||
| chr2:48352655 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.537+5904C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48352655 | |||||||
| chr2:48352916 | G | T | 1 | a0001c0002t0002g0286 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.538-6131G>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48352916 | |||||||
| chr2:48353045 | G | T | 1 | a0001c0003t0016g0135 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.538-6002G>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48353045 | |||||||
| chr2:48353066 | G | C | 5 | a0001c0001t0001g0141 a0001c0001t0001g0162 a0001c0001t0001g0188 others(2): Show |
5 | HG02145.hp1 HG02809.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.538-5981G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48353066 | |||||||
| chr2:48353156 | A | T | 1 | a0001c0001t0001g0121 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.538-5891A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48353156 | |||||||
| chr2:48353157 | T | A | 1 | a0001c0001t0001g0121 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.538-5890T>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48353157 | |||||||
| chr2:48353221 | C | A | 1 | a0001c0002t0002g0295 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.538-5826C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48353221 | |||||||
| chr2:48353378 | G | A | 1 | a0001c0002t0002g0306 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.538-5669G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48353378 | |||||||
| chr2:48353416 | A | G | 6 | a0001c0002t0002g0009 a0001c0002t0002g0287 a0001c0002t0002g0317 others(3): Show |
7 | HG02056.hp1 HG02135.hp2 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.538-5631A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48353416 | |||||||
| chr2:48353506 | T | G | 113 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(110): Show |
115 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.538-5541T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48353506 | |||||||
| chr2:48353552 | CTG | C | 33 | a0001c0001t0001g0013 a0001c0001t0001g0070 a0001c0001t0001g0079 others(30): Show |
34 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.538-5442_538-5441d others(4): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48353552 | ||||||
| chr2:48353552 | CTGTG | C | 53 | a0001c0001t0001g0050 a0001c0001t0001g0058 a0001c0001t0001g0064 others(50): Show |
53 | HG00408.hp2 HG00558.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.538-5444_538-5441d others(6): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48353552 | ||||||
| chr2:48353552 | CTGTGTG | C | 107 | a0001c0001t0001g0007 a0001c0001t0001g0049 a0001c0001t0001g0052 others(104): Show |
113 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.538-5446_538-5441d others(8): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48353552 | ||||||
| chr2:48353552 | CTGTGTGT others(1): Show |
C | 55 | a0001c0001t0001g0012 a0001c0001t0001g0051 a0001c0001t0001g0053 others(52): Show |
55 | HG00280.hp2 HG00639.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.538-5448_538-5441d others(10): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48353552 | ||||||
| chr2:48353552 | CTGTGTGT others(3): Show |
C | 35 | a0001c0001t0001g0076 a0001c0001t0001g0093 a0001c0001t0001g0161 others(32): Show |
37 | HG01069.hp1 HG01109.hp2 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.538-5450_538-5441d others(12): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48353552 | ||||||
| chr2:48353552 | CTGTGTGT others(5): Show |
C | 13 | a0001c0001t0001g0014 a0001c0001t0001g0092 a0001c0001t0001g0097 others(10): Show |
13 | HG00099.hp2 HG00738.hp2 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.538-5452_538-5441d others(14): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48353552 | ||||||
| chr2:48353552 | CTGTGTGT others(7): Show |
C | 3 | a0001c0001t0001g0157 a0001c0002t0002g0260 a0001c0003t0007g0010 |
3 | HG02717.hp1 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.538-5454_538-5441d others(16): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48353552 | ||||||
| chr2:48353552 | CTGTGTGT others(9): Show |
C | 9 | a0001c0002t0006g0237 a0001c0002t0006g0239 a0001c0002t0006g0240 others(6): Show |
9 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.538-5456_538-5441d others(18): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48353552 | ||||||
| chr2:48353552 | CTGTGTGT others(15): Show |
C | 1 | a0001c0001t0001g0060 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.538-5462_538-5441d others(24): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48353552 | ||||||
| chr2:48353552 | CTGTGTGT others(19): Show |
C | 1 | a0001c0001t0001g0232 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.538-5466_538-5441d others(28): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48353552 | ||||||
| chr2:48353605 | T | A | 27 | a0001c0001t0002g0017 a0001c0001t0002g0030 a0001c0001t0002g0034 others(24): Show |
30 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.538-5442T>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48353605 | |||||||
| chr2:48353605 | T | TGA | 5 | a0001c0001t0002g0022 a0001c0001t0005g0003 a0001c0001t0005g0026 others(2): Show |
6 | HG01433.hp2 HG01891.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.538-5441_538-5440d others(4): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48353605 | ||||||
| chr2:48353619 | G | C | 1 | a0001c0001t0004g0081 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.538-5428G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48353619 | |||||||
| chr2:48353855 | T | A | 1 | a0001c0001t0002g0038 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.538-5192T>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48353855 | |||||||
| chr2:48354219 | C | G | 1 | a0001c0002t0003g0256 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.538-4828C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48354219 | |||||||
| chr2:48354335 | C | A | 1 | a0001c0001t0014g0160 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.538-4712C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48354335 | |||||||
| chr2:48354339 | C | T | 2 | a0001c0001t0001g0229 a0001c0001t0001g0233 |
2 | HG00099.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.538-4708C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48354339 | |||||||
| chr2:48354367 | T | C | 206 | a0001c0001t0001g0014 a0001c0001t0001g0051 a0001c0001t0001g0052 others(203): Show |
212 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.538-4680T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48354367 | |||||||
| chr2:48354367 | T | G | 7 | a0001c0001t0001g0007 a0001c0001t0001g0050 a0001c0001t0001g0144 others(4): Show |
8 | HG02109.hp2 HG02280.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.538-4680T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48354367 | |||||||
| chr2:48354585 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.538-4462C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48354585 | |||||||
| chr2:48354593 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.538-4454C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48354593 | |||||||
| chr2:48354649 | A | G | 2 | a0001c0001t0001g0013 a0001c0001t0004g0006 |
3 | NA18960.hp1 NA18998.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.538-4398A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48354649 | |||||||
| chr2:48354737 | T | C | 150 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(147): Show |
156 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.538-4310T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48354737 | |||||||
| chr2:48354805 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.538-4242A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48354805 | |||||||
| chr2:48354999 | G | A | 2 | a0001c0002t0003g0015 a0001c0002t0003g0257 |
2 | HG02717.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.538-4048G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48354999 | |||||||
| chr2:48355159 | A | G | 11 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0003 others(8): Show |
13 | HG01433.hp2 HG01891.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.538-3888A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48355159 | |||||||
| chr2:48355171 | G | A | 1 | a0001c0002t0002g0284 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.538-3876G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48355171 | |||||||
| chr2:48355189 | G | T | 1 | a0001c0002t0002g0327 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.538-3858G>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48355189 | |||||||
| chr2:48355201 | T | C | 1 | a0001c0001t0001g0129 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.538-3846T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48355201 | |||||||
| chr2:48355401 | T | C | 10 | a0001c0002t0003g0015 a0001c0002t0003g0246 a0001c0002t0003g0248 others(7): Show |
10 | HG00738.hp2 HG01109.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.538-3646T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48355401 | |||||||
| chr2:48355430 | C | T | 1 | a0001c0001t0001g0178 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.538-3617C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48355430 | |||||||
| chr2:48355511 | G | A | 88 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0220 others(85): Show |
90 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.538-3536G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48355511 | |||||||
| chr2:48355566 | T | A | 3 | a0001c0001t0001g0205 a0001c0003t0007g0010 a0001c0003t0007g0011 |
3 | HG01106.hp1 HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.538-3481T>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48355566 | |||||||
| chr2:48355606 | G | A | 98 | a0001c0001t0001g0214 a0001c0001t0001g0231 a0001c0001t0001g0323 others(95): Show |
100 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.538-3441G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48355606 | |||||||
| chr2:48355815 | C | G | 11 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0003 others(8): Show |
13 | HG01433.hp2 HG01891.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.538-3232C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48355815 | |||||||
| chr2:48355818 | TATC | T | 3 | a0001c0002t0003g0250 a0001c0002t0003g0251 a0001c0002t0003g0252 |
3 | HG03225.hp2 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.538-3223_538-3221d others(5): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48355818 | ||||||
| chr2:48356283 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.538-2764A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48356283 | |||||||
| chr2:48356324 | C | T | 6 | a0001c0003t0001g0133 a0001c0003t0001g0134 a0001c0003t0001g0136 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.538-2723C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48356324 | |||||||
| chr2:48356325 | C | A | 1 | a0001c0002t0002g0271 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.538-2722C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48356325 | |||||||
| chr2:48356406 | A | G | 150 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(147): Show |
156 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.538-2641A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48356406 | |||||||
| chr2:48356460 | C | T | 86 | a0001c0001t0001g0214 a0001c0001t0001g0231 a0001c0001t0001g0323 others(83): Show |
88 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.538-2587C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48356460 | |||||||
| chr2:48356582 | AATT | A | 98 | a0001c0001t0001g0214 a0001c0001t0001g0231 a0001c0001t0001g0323 others(95): Show |
100 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.538-2461_538-2459d others(5): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48356582 | ||||||
| chr2:48356703 | A | C | 1 | a0001c0002t0002g0320 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.538-2344A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48356703 | |||||||
| chr2:48356852 | C | T | 41 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0219 others(38): Show |
45 | HG00099.hp1 HG01069.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.538-2195C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48356852 | |||||||
| chr2:48356855 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.538-2192C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48356855 | |||||||
| chr2:48357020 | A | G | 8 | a0001c0002t0006g0237 a0001c0002t0006g0239 a0001c0002t0006g0240 others(5): Show |
8 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.538-2027A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48357020 | |||||||
| chr2:48357163 | G | A | 149 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(146): Show |
155 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.538-1884G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48357163 | |||||||
| chr2:48357335 | A | G | 98 | a0001c0001t0001g0214 a0001c0001t0001g0231 a0001c0001t0001g0323 others(95): Show |
100 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.538-1712A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48357335 | |||||||
| chr2:48357436 | C | G | 120 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(117): Show |
122 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.538-1611C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48357436 | |||||||
| chr2:48357453 | G | C | 1 | a0001c0001t0001g0156 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.538-1594G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48357453 | |||||||
| chr2:48357504 | C | CT | 8 | a0001c0002t0006g0237 a0001c0002t0006g0239 a0001c0002t0006g0240 others(5): Show |
8 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.538-1530dupT | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48357504 | ||||||
| chr2:48357687 | C | T | 106 | a0001c0001t0001g0214 a0001c0001t0001g0231 a0001c0001t0001g0323 others(103): Show |
108 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.538-1360C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48357687 | |||||||
| chr2:48357705 | G | A | 1 | a0001c0002t0002g0295 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.538-1342G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48357705 | |||||||
| chr2:48357802 | T | C | 10 | a0001c0002t0003g0015 a0001c0002t0003g0246 a0001c0002t0003g0248 others(7): Show |
10 | HG00738.hp2 HG01109.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.538-1245T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48357802 | |||||||
| chr2:48357862 | GA | G | 7 | a0001c0001t0001g0054 a0001c0001t0001g0121 a0001c0001t0001g0159 others(4): Show |
7 | HG02738.hp2 HG02965.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.538-1166delA | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48357862 | ||||||
| chr2:48357862 | GAA | G | 29 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0219 others(26): Show |
31 | HG00099.hp1 HG01069.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.538-1167_538-1166d others(4): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48357862 | ||||||
| chr2:48357862 | GAAA | G | 109 | a0001c0001t0001g0214 a0001c0001t0001g0231 a0001c0001t0001g0323 others(106): Show |
113 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.538-1168_538-1166d others(5): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48357862 | ||||||
| chr2:48357862 | GAAAA | G | 8 | a0001c0002t0006g0237 a0001c0002t0006g0239 a0001c0002t0006g0240 others(5): Show |
8 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.538-1169_538-1166d others(6): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48357862 | ||||||
| chr2:48357906 | A | G | 8 | a0001c0002t0006g0237 a0001c0002t0006g0239 a0001c0002t0006g0240 others(5): Show |
8 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.538-1141A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48357906 | |||||||
| chr2:48357958 | A | G | 1 | a0001c0002t0002g0036 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.538-1089A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48357958 | |||||||
| chr2:48358019 | A | G | 98 | a0001c0001t0001g0214 a0001c0001t0001g0231 a0001c0001t0001g0323 others(95): Show |
100 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.538-1028A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48358019 | |||||||
| chr2:48358036 | T | G | 4 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(1): Show |
4 | HG00738.hp1 HG01106.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.538-1011T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48358036 | |||||||
| chr2:48358312 | G | A | 3 | a0001c0002t0002g0266 a0001c0002t0002g0333 a0001c0002t0002g0334 |
3 | HG01106.hp2 HG01109.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.538-735G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48358312 | |||||||
| chr2:48358367 | C | T | 107 | a0001c0001t0001g0214 a0001c0001t0001g0231 a0001c0001t0001g0323 others(104): Show |
109 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.538-680C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48358367 | |||||||
| chr2:48358443 | A | G | 10 | a0001c0001t0001g0007 a0001c0001t0001g0050 a0001c0001t0001g0144 others(7): Show |
11 | HG02109.hp2 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.538-604A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48358443 | |||||||
| chr2:48358449 | T | C | 2 | a0001c0001t0001g0095 a0001c0001t0001g0096 |
2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.538-598T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48358449 | |||||||
| chr2:48358499 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.538-548C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48358499 | |||||||
| chr2:48358673 | A | G | 5 | a0001c0002t0003g0246 a0001c0002t0003g0248 a0001c0002t0003g0249 others(2): Show |
5 | HG00738.hp2 HG01109.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.538-374A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48358673 | |||||||
| chr2:48358824 | A | C | 41 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0219 others(38): Show |
45 | HG00099.hp1 HG01069.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.538-223A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48358824 | |||||||
| chr2:48358880 | AATCC | A | 146 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0219 others(143): Show |
152 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.538-166_538-163del others(4): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48358880 | |||||||
| chr2:48358883 | C | A | 1 | a0001c0001t0001g0089 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.538-164C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48358883 | |||||||
| chr2:48358884 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.538-163C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48358884 | |||||||
| chr2:48358895 | C | G | 116 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0219 others(113): Show |
118 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.538-152C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48358895 | |||||||
| chr2:48358926 | C | T | 11 | a0001c0002t0003g0015 a0001c0002t0003g0246 a0001c0002t0003g0248 others(8): Show |
11 | HG00738.hp2 HG01109.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.538-121C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48358926 | |||||||
| chr2:48359001 | G | C | 1 | a0001c0002t0002g0294 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.538-46G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48359001 | |||||||
| chr2:48359225 | G | A | 1 | a0001c0002t0002g0295 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.638+78G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48359225 | |||||||
| chr2:48359226 | G | A | 4 | a0001c0001t0001g0110 a0001c0001t0001g0112 a0001c0001t0001g0170 others(1): Show |
4 | HG01099.hp1 HG01175.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.638+79G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48359226 | |||||||
| chr2:48359264 | T | C | 3 | a0001c0002t0003g0015 a0001c0002t0003g0256 a0001c0002t0003g0257 |
3 | HG02717.hp2 HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.638+117T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48359264 | |||||||
| chr2:48359270 | ATTTAGTT | A | 105 | a0001c0001t0001g0323 a0001c0002t0002g0008 a0001c0002t0002g0009 others(102): Show |
107 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.638+141_638+147del others(7): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 48359270 | ||||||
| chr2:48359355 | G | C | 1 | a0001c0001t0001g0128 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.638+208G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48359355 | |||||||
| chr2:48359358 | A | T | 1 | a0001c0002t0002g0325 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.638+211A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48359358 | |||||||
| chr2:48359403 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.638+256C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48359403 | |||||||
| chr2:48359499 | G | A | 1 | a0001c0001t0001g0064 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.638+352G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48359499 | |||||||
| chr2:48359549 | C | T | 1 | a0001c0002t0003g0257 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.638+402C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48359549 | |||||||
| chr2:48359563 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.638+416G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48359563 | |||||||
| chr2:48359574 | G | A | 8 | a0001c0002t0006g0237 a0001c0002t0006g0239 a0001c0002t0006g0240 others(5): Show |
8 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.638+427G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48359574 | |||||||
| chr2:48359586 | C | A | 7 | a0001c0003t0001g0133 a0001c0003t0001g0134 a0001c0003t0001g0136 others(4): Show |
7 | HG01884.hp2 HG02109.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.638+439C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48359586 | |||||||
| chr2:48359597 | TTTTTCTT others(3): Show |
T | 2 | a0001c0003t0016g0135 a0004c0006t0001g0063 |
2 | HG03130.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.638+470_638+479del others(10): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 48359597 | ||||||
| chr2:48359622 | C | CTTTTT | 94 | a0001c0001t0001g0323 a0001c0002t0002g0008 a0001c0002t0002g0009 others(91): Show |
96 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.638+478_638+482dup others(5): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 48359622 | ||||||
| chr2:48359622 | C | T | 49 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0219 others(46): Show |
53 | HG00099.hp1 HG00280.hp1 HG01069.hp1 others(50): Show |
intron_variant | MODIFIER | c.638+475C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48359622 | |||||||
| chr2:48359925 | T | A | 1 | a0001c0001t0001g0173 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.638+778T>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48359925 | |||||||
| chr2:48360015 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.638+868A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48360015 | |||||||
| chr2:48360059 | A | G | 106 | a0001c0001t0001g0215 a0001c0001t0001g0220 a0001c0002t0002g0008 others(103): Show |
108 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.638+912A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48360059 | |||||||
| chr2:48360200 | C | G | 1 | a0001c0001t0002g0022 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.638+1053C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48360200 | |||||||
| chr2:48360547 | C | G | 44 | a0001c0001t0001g0154 a0001c0001t0001g0157 a0001c0001t0001g0199 others(41): Show |
48 | HG00099.hp1 HG01069.hp1 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.638+1400C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48360547 | |||||||
| chr2:48360602 | A | G | 85 | a0001c0001t0001g0215 a0001c0001t0001g0220 a0001c0002t0002g0008 others(82): Show |
87 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.638+1455A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48360602 | |||||||
| chr2:48360680 | A | G | 13 | a0001c0002t0003g0015 a0001c0002t0003g0246 a0001c0002t0003g0248 others(10): Show |
13 | HG00738.hp2 HG01109.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.638+1533A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48360680 | |||||||
| chr2:48360776 | C | T | 1 | a0001c0001t0005g0029 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.638+1629C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48360776 | |||||||
| chr2:48360790 | G | GT | 16 | a0001c0001t0001g0115 a0001c0001t0001g0121 a0001c0001t0001g0177 others(13): Show |
16 | HG00408.hp2 HG00438.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.638+1658dupT | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 48360790 | ||||||
| chr2:48360824 | A | T | 32 | a0001c0001t0001g0098 a0001c0001t0001g0101 a0001c0001t0001g0108 others(29): Show |
32 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.638+1677A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48360824 | |||||||
| chr2:48360918 | G | A | 8 | a0001c0002t0003g0246 a0001c0002t0003g0248 a0001c0002t0003g0249 others(5): Show |
8 | HG00738.hp2 HG01109.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.639-1725G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48360918 | |||||||
| chr2:48361013 | CA | C | 146 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0219 others(143): Show |
152 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.639-1616delA | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 48361013 | ||||||
| chr2:48361058 | G | C | 146 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0219 others(143): Show |
152 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.639-1585G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48361058 | |||||||
| chr2:48361128 | A | C | 1 | a0001c0001t0001g0162 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.639-1515A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48361128 | |||||||
| chr2:48361416 | G | A | 3 | a0001c0002t0003g0015 a0001c0002t0003g0256 a0001c0002t0003g0257 |
3 | HG02717.hp2 HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.639-1227G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48361416 | |||||||
| chr2:48361438 | G | A | 10 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0003t0001g0133 others(7): Show |
10 | HG01074.hp1 HG01884.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.639-1205G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48361438 | |||||||
| chr2:48361826 | A | C | 1 | a0001c0003t0001g0137 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.639-817A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48361826 | |||||||
| chr2:48361841 | A | G | 1 | a0001c0002t0003g0257 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.639-802A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48361841 | |||||||
| chr2:48362027 | A | C | 150 | a0001c0001t0001g0172 a0001c0001t0001g0215 a0001c0001t0001g0216 others(147): Show |
156 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.639-616A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48362027 | |||||||
| chr2:48362165 | C | A | 1 | a0001c0001t0001g0218 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.639-478C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48362165 | |||||||
| chr2:48362259 | A | G | 1 | a0001c0002t0002g0285 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.639-384A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48362259 | |||||||
| chr2:48362287 | G | C | 1 | a0001c0002t0002g0258 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.639-356G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48362287 | |||||||
| chr2:48362511 | G | C | 1 | a0001c0002t0003g0091 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.639-132G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48362511 | |||||||
| chr2:48362544 | G | A | 17 | a0001c0001t0001g0012 a0001c0001t0001g0099 a0001c0001t0001g0102 others(14): Show |
17 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.639-99G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48362544 | |||||||
| chr2:48362570 | C | A | 1 | a0001c0002t0002g0295 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.639-73C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48362570 | |||||||
| chr2:48362782 | G | T | 1 | a0001c0001t0001g0107 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.703+75G>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48362782 | |||||||
| chr2:48362790 | C | A | 1 | a0001c0001t0001g0093 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.703+83C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48362790 | |||||||
| chr2:48362852 | T | C | 1 | a0001c0001t0014g0160 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.703+145T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48362852 | |||||||
| chr2:48362879 | T | A | 1 | a0001c0003t0001g0137 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.703+172T>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48362879 | |||||||
| chr2:48363028 | G | A | 2 | a0001c0002t0002g0275 a0001c0002t0002g0288 |
2 | HG03834.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.703+321G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48363028 | |||||||
| chr2:48363074 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.703+367C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48363074 | |||||||
| chr2:48363131 | T | C | 293 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0014 others(290): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.703+424T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48363131 | |||||||
| chr2:48363210 | G | T | 2 | a0001c0001t0001g0122 a0001c0001t0020g0116 |
2 | HG01952.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.703+503G>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48363210 | |||||||
| chr2:48363238 | G | A | 1 | a0001c0001t0004g0055 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.703+531G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48363238 | |||||||
| chr2:48363385 | AG | A | 38 | a0001c0001t0001g0098 a0001c0001t0001g0101 a0001c0001t0001g0108 others(35): Show |
38 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.703+679delG | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48363385 | |||||||
| chr2:48363423 | T | C | 1 | a0001c0001t0001g0203 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.703+716T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48363423 | |||||||
| chr2:48363987 | A | G | 2 | a0001c0001t0001g0214 a0001c0001t0001g0231 |
2 | HG02602.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.703+1280A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48363987 | |||||||
| chr2:48364071 | A | C | 1 | a0001c0001t0001g0132 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.703+1364A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48364071 | |||||||
| chr2:48364162 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.703+1455G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48364162 | |||||||
| chr2:48364290 | C | G | 1 | a0001c0002t0002g0260 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.703+1583C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48364290 | |||||||
| chr2:48364468 | G | A | 98 | a0001c0001t0018g0105 a0001c0002t0002g0008 a0001c0002t0002g0009 others(95): Show |
100 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.703+1761G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48364468 | |||||||
| chr2:48364553 | C | T | 10 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0023 others(7): Show |
12 | HG01433.hp2 HG01891.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.703+1846C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48364553 | |||||||
| chr2:48364619 | A | G | 1 | a0001c0001t0002g0039 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.703+1912A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48364619 | |||||||
| chr2:48364637 | G | C | 3 | a0001c0002t0002g0264 a0001c0002t0002g0276 a0001c0002t0002g0320 |
3 | NA18942.hp1 NA19000.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.703+1930G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48364637 | |||||||
| chr2:48364750 | G | C | 40 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0219 others(37): Show |
42 | HG00099.hp1 HG01069.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.703+2043G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48364750 | |||||||
| chr2:48364830 | C | T | 1 | a0001c0001t0012g0044 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.703+2123C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48364830 | |||||||
| chr2:48364871 | C | A | 2 | a0001c0001t0001g0095 a0001c0001t0001g0096 |
2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.703+2164C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48364871 | |||||||
| chr2:48364947 | T | C | 1 | a0001c0001t0002g0022 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.703+2240T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48364947 | |||||||
| chr2:48365002 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.703+2295A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48365002 | |||||||
| chr2:48365010 | T | C | 1 | a0001c0001t0004g0061 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.703+2303T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48365010 | |||||||
| chr2:48365023 | G | A | 2 | a0001c0002t0010g0245 a0001c0002t0010g0247 |
2 | HG01109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.703+2316G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48365023 | |||||||
| chr2:48365028 | T | G | 1 | a0001c0004t0003g0043 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.703+2321T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48365028 | |||||||
| chr2:48365063 | T | C | 97 | a0001c0001t0018g0105 a0001c0002t0002g0008 a0001c0002t0002g0009 others(94): Show |
99 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.703+2356T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48365063 | |||||||
| chr2:48365085 | G | A | 138 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0219 others(135): Show |
142 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.703+2378G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48365085 | |||||||
| chr2:48365102 | C | T | 85 | a0001c0001t0018g0105 a0001c0002t0002g0008 a0001c0002t0002g0009 others(82): Show |
87 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.703+2395C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48365102 | |||||||
| chr2:48365430 | T | C | 39 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0219 others(36): Show |
41 | HG00099.hp1 HG01069.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.703+2723T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48365430 | |||||||
| chr2:48365469 | T | A | 1 | a0001c0001t0001g0199 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.703+2762T>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48365469 | |||||||
| chr2:48365574 | G | C | 1 | a0001c0001t0001g0255 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.703+2867G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48365574 | |||||||
| chr2:48365615 | T | C | 13 | a0001c0001t0002g0016 a0001c0001t0002g0032 a0001c0001t0002g0038 others(10): Show |
13 | HG01069.hp1 HG01167.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.703+2908T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48365615 | |||||||
| chr2:48365627 | A | G | 1 | a0001c0002t0002g0260 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.703+2920A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48365627 | |||||||
| chr2:48365639 | G | A | 1 | a0001c0003t0016g0135 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.703+2932G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48365639 | |||||||
| chr2:48365658 | T | C | 1 | a0001c0001t0001g0013 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.703+2951T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48365658 | |||||||
| chr2:48365663 | C | G | 8 | a0001c0002t0006g0237 a0001c0002t0006g0239 a0001c0002t0006g0240 others(5): Show |
8 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.703+2956C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48365663 | |||||||
| chr2:48365693 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.703+2986C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48365693 | |||||||
| chr2:48365938 | A | G | 56 | a0001c0001t0018g0105 a0001c0002t0002g0008 a0001c0002t0002g0009 others(53): Show |
58 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.703+3231A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48365938 | |||||||
| chr2:48366025 | A | G | 1 | a0001c0001t0002g0030 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.703+3318A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48366025 | |||||||
| chr2:48366080 | G | A | 40 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0219 others(37): Show |
42 | HG00099.hp1 HG01069.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.703+3373G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48366080 | |||||||
| chr2:48366085 | A | G | 140 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(137): Show |
144 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.703+3378A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48366085 | |||||||
| chr2:48366108 | G | A | 1 | a0001c0002t0003g0091 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.703+3401G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48366108 | |||||||
| chr2:48366134 | A | G | 8 | a0001c0002t0006g0237 a0001c0002t0006g0239 a0001c0002t0006g0240 others(5): Show |
8 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.703+3427A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48366134 | |||||||
| chr2:48366353 | C | CA | 10 | a0001c0001t0001g0085 a0001c0001t0001g0089 a0001c0001t0001g0121 others(7): Show |
10 | HG00099.hp1 HG00733.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.703+3664dupA | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 48366353 | ||||||
| chr2:48366353 | CA | C | 100 | a0001c0001t0018g0105 a0001c0002t0002g0008 a0001c0002t0002g0009 others(97): Show |
102 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.703+3664delA | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 48366353 | ||||||
| chr2:48366577 | A | G | 1 | a0001c0002t0002g0295 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.703+3870A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48366577 | |||||||
| chr2:48366608 | C | A | 1 | a0001c0001t0001g0209 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.703+3901C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48366608 | |||||||
| chr2:48366662 | A | G | 40 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0219 others(37): Show |
42 | HG00099.hp1 HG01069.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.703+3955A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48366662 | |||||||
| chr2:48367171 | C | G | 80 | a0001c0001t0001g0215 a0001c0001t0001g0220 a0001c0001t0018g0105 others(77): Show |
82 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.703+4464C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48367171 | |||||||
| chr2:48367198 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.703+4491C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48367198 | |||||||
| chr2:48367216 | A | G | 41 | a0001c0001t0001g0153 a0001c0001t0001g0216 a0001c0001t0001g0217 others(38): Show |
43 | HG00099.hp1 HG01069.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.703+4509A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48367216 | |||||||
| chr2:48367456 | C | T | 141 | a0001c0001t0001g0153 a0001c0001t0001g0215 a0001c0001t0001g0216 others(138): Show |
145 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.703+4749C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48367456 | |||||||
| chr2:48367728 | A | T | 1 | a0001c0003t0001g0137 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.703+5021A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48367728 | |||||||
| chr2:48367748 | T | C | 87 | a0001c0001t0001g0215 a0001c0001t0001g0220 a0001c0001t0018g0105 others(84): Show |
89 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.703+5041T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48367748 | |||||||
| chr2:48367826 | A | G | 141 | a0001c0001t0001g0153 a0001c0001t0001g0215 a0001c0001t0001g0216 others(138): Show |
145 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.703+5119A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48367826 | |||||||
| chr2:48368158 | C | T | 1 | a0001c0002t0003g0256 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.704-5134C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48368158 | |||||||
| chr2:48368253 | A | AAT | 28 | a0001c0002t0003g0015 a0001c0002t0003g0091 a0001c0002t0003g0246 others(25): Show |
30 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.704-5037_704-5036d others(4): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 48368253 | ||||||
| chr2:48368292 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.704-5000A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48368292 | |||||||
| chr2:48368351 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.704-4941A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48368351 | |||||||
| chr2:48368767 | A | T | 1 | a0001c0001t0001g0062 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.704-4525A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48368767 | |||||||
| chr2:48368779 | C | A | 8 | a0001c0002t0006g0237 a0001c0002t0006g0239 a0001c0002t0006g0240 others(5): Show |
8 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.704-4513C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48368779 | |||||||
| chr2:48368797 | T | A | 1 | a0001c0001t0001g0104 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.704-4495T>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48368797 | |||||||
| chr2:48368843 | T | G | 2 | a0001c0002t0002g0299 a0001c0002t0002g0300 |
2 | NA19004.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.704-4449T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48368843 | |||||||
| chr2:48369034 | A | G | 2 | a0001c0001t0008g0100 a0001c0001t0008g0111 |
2 | HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.704-4258A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48369034 | |||||||
| chr2:48369082 | C | T | 1 | a0001c0002t0002g0289 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.704-4210C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48369082 | |||||||
| chr2:48369097 | G | A | 1 | a0002c0005t0001g0094 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.704-4195G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48369097 | |||||||
| chr2:48369373 | A | C | 1 | a0001c0001t0001g0191 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.704-3919A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48369373 | |||||||
| chr2:48369395 | G | A | 1 | a0001c0001t0002g0035 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.704-3897G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48369395 | |||||||
| chr2:48369434 | A | C | 17 | a0001c0001t0001g0101 a0001c0001t0001g0108 a0001c0001t0001g0114 others(14): Show |
17 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(14): Show |
intron_variant | MODIFIER | c.704-3858A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48369434 | |||||||
| chr2:48369504 | C | T | 1 | a0001c0002t0002g0313 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.704-3788C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48369504 | |||||||
| chr2:48369517 | G | C | 1 | a0001c0001t0001g0177 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.704-3775G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48369517 | |||||||
| chr2:48369696 | A | G | 1 | a0001c0002t0002g0271 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.704-3596A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48369696 | |||||||
| chr2:48369710 | C | T | 2 | a0001c0001t0001g0138 a0001c0001t0001g0147 |
2 | HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.704-3582C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48369710 | |||||||
| chr2:48369811 | C | G | 84 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0031 others(81): Show |
86 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.704-3481C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48369811 | |||||||
| chr2:48369813 | C | T | 1 | a0001c0002t0022g0238 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.704-3479C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48369813 | |||||||
| chr2:48369823 | A | G | 84 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0031 others(81): Show |
86 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.704-3469A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48369823 | |||||||
| chr2:48369848 | A | G | 1 | a0001c0002t0002g0305 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.704-3444A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48369848 | |||||||
| chr2:48369862 | C | T | 1 | a0001c0002t0002g0286 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.704-3430C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48369862 | |||||||
| chr2:48369880 | G | A | 1 | a0001c0002t0002g0300 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.704-3412G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48369880 | |||||||
| chr2:48369906 | T | G | 112 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0031 others(109): Show |
116 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.704-3386T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48369906 | |||||||
| chr2:48370156 | C | T | 84 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0031 others(81): Show |
86 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.704-3136C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48370156 | |||||||
| chr2:48370244 | A | G | 1 | a0001c0001t0002g0035 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.704-3048A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48370244 | |||||||
| chr2:48370328 | ATTGGAGA others(10): Show |
A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0236 |
2 | HG00733.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.704-2961_704-2945d others(19): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 48370328 | ||||||
| chr2:48370417 | C | A | 4 | a0001c0001t0001g0151 a0001c0001t0001g0155 a0001c0001t0001g0182 others(1): Show |
4 | HG00733.hp2 HG01167.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-2875C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48370417 | |||||||
| chr2:48370420 | G | A | 136 | a0001c0001t0001g0153 a0001c0001t0001g0216 a0001c0001t0001g0217 others(133): Show |
140 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.704-2872G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48370420 | |||||||
| chr2:48370660 | G | C | 95 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0031 others(92): Show |
99 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.704-2632G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48370660 | |||||||
| chr2:48370812 | G | A | 1 | a0003c0007t0013g0145 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.704-2480G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48370812 | |||||||
| chr2:48371362 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.704-1930C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48371362 | |||||||
| chr2:48371429 | T | C | 1 | a0001c0002t0003g0091 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.704-1863T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48371429 | |||||||
| chr2:48371431 | A | G | 12 | a0001c0002t0003g0015 a0001c0002t0003g0091 a0001c0002t0003g0246 others(9): Show |
12 | HG00738.hp2 HG01109.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.704-1861A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48371431 | |||||||
| chr2:48371538 | T | C | 146 | a0001c0001t0001g0153 a0001c0001t0001g0216 a0001c0001t0001g0217 others(143): Show |
152 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.704-1754T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48371538 | |||||||
| chr2:48371710 | C | G | 77 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0031 others(74): Show |
79 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.704-1582C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48371710 | |||||||
| chr2:48371743 | G | A | 134 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0022 others(131): Show |
140 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.704-1549G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48371743 | |||||||
| chr2:48372120 | A | C | 1 | a0001c0002t0002g0317 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.704-1172A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48372120 | |||||||
| chr2:48372123 | C | T | 2 | a0001c0002t0002g0296 a0001c0002t0002g0327 |
2 | NA18975.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.704-1169C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48372123 | |||||||
| chr2:48372249 | C | T | 8 | a0001c0002t0006g0237 a0001c0002t0006g0239 a0001c0002t0006g0240 others(5): Show |
8 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.704-1043C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48372249 | |||||||
| chr2:48372263 | A | C | 3 | a0001c0001t0004g0005 a0001c0001t0004g0080 a0001c0001t0004g0086 |
4 | NA19004.hp2 NA19064.hp1 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.704-1029A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48372263 | |||||||
| chr2:48372484 | A | G | 2 | a0001c0001t0001g0106 a0001c0001t0001g0254 |
2 | HG00639.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.704-808A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48372484 | |||||||
| chr2:48372512 | A | G | 1 | a0001c0004t0003g0019 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.704-780A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48372512 | |||||||
| chr2:48372892 | A | G | 11 | a0001c0001t0001g0007 a0001c0001t0001g0050 a0001c0001t0001g0144 others(8): Show |
12 | HG01346.hp1 HG02109.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.704-400A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48372892 | |||||||
| chr2:48372922 | CA | C | 27 | a0001c0001t0001g0153 a0001c0001t0001g0216 a0001c0001t0001g0217 others(24): Show |
27 | HG00099.hp1 HG01069.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.704-356delA | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 48372922 | ||||||
| chr2:48373012 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.704-280G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48373012 | |||||||
| chr2:48373073 | T | C | 2 | a0001c0002t0002g0333 a0001c0002t0002g0334 |
2 | HG01106.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.704-219T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48373073 | |||||||
| chr2:48373103 | G | A | 1 | a0001c0001t0001g0209 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.704-189G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48373103 | |||||||
| chr2:48373190 | A | G | 1 | a0001c0001t0004g0065 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.704-102A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48373190 | |||||||
| chr2:48373381 | T | A | 1 | a0001c0001t0002g0030 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.772+21T>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 6/6 | chr2 | 48373381 | |||||||
| chr2:48373390 | A | T | 1 | a0001c0001t0002g0035 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.772+30A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 6/6 | chr2 | 48373390 | |||||||
| chr2:48373494 | CTGTTT | C | 3 | a0001c0002t0003g0015 a0001c0002t0003g0256 a0001c0002t0003g0257 |
3 | HG02717.hp2 HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.772+136_772+140del others(5): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 48373494 | ||||||
| chr2:48373552 | T | G | 134 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0022 others(131): Show |
140 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.772+192T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 6/6 | chr2 | 48373552 | |||||||
| chr2:48373553 | C | T | 134 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0022 others(131): Show |
140 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.772+193C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 6/6 | chr2 | 48373553 | |||||||
| chr2:48373918 | G | A | 1 | a0001c0002t0009g0280 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.772+558G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 6/6 | chr2 | 48373918 | |||||||
| chr2:48373947 | C | G | 1 | a0001c0001t0001g0161 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.772+587C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 6/6 | chr2 | 48373947 | |||||||
| chr2:48373992 | TTGCAGTG others(12): Show |
T | 2 | a0001c0001t0001g0138 a0001c0001t0001g0147 |
2 | HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.772+643_772+661del others(19): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 48373992 | ||||||
| chr2:48374166 | A | G | 6 | a0001c0001t0001g0098 a0001c0001t0001g0150 a0001c0001t0001g0165 others(3): Show |
6 | HG00733.hp1 HG01981.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.773-754A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 6/6 | chr2 | 48374166 | |||||||
| chr2:48374309 | G | T | 134 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0022 others(131): Show |
140 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.773-611G>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 6/6 | chr2 | 48374309 | |||||||
| chr2:48374359 | G | C | 1 | a0001c0002t0003g0091 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.773-561G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 6/6 | chr2 | 48374359 | |||||||
| chr2:48374381 | T | A | 2 | a0001c0002t0002g0297 a0001c0002t0002g0311 |
2 | NA18991.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.773-539T>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 6/6 | chr2 | 48374381 | |||||||
| chr2:48374589 | G | C | 1 | a0001c0001t0001g0232 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.773-331G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 6/6 | chr2 | 48374589 | |||||||
| chr2:48374677 | C | T | 134 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0022 others(131): Show |
140 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.773-243C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 6/6 | chr2 | 48374677 | |||||||
| chr2:48374702 | A | C | 1 | a0001c0002t0002g0260 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.773-218A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 6/6 | chr2 | 48374702 | |||||||
| chr2:48374719 | C | G | 1 | a0001c0001t0019g0168 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.773-201C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 6/6 | chr2 | 48374719 |